FDA event 65707 · Recall Observatory

drug · product 1 of 273

ZINC GLUCONATE, Tablet, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904319160.

D-463-2014

Recall number: D-463-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ZINC GLUCONATE, Tablet, 50 mg may be potentially mis-labeled as ASCORBIC ACID, Chew Tablet, 500 mg, NDC 00904052660, Pedigree: AD60240_54, EXP: 5/22/2014 and ASCORBIC ACID, Chew Tablet, 250 mg, NDC 00904052260, Pedigree: W003027, EXP: 6/12/2014.

Code information

ZINC GLUCONATE, Tablet, 50 mg has the following codes: Pedigree: AD60240_57, EXP: 5/22/2014; Pedigree: W003028, EXP: 6/12/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 2 of 273

CALCIUM CARBONATE +D3, Tablet, 600 mg/400 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904323392.

D-464-2014

Recall number: D-464-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 10,819 tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CALCIUM CARBONATE +D3, Tablet, 600 mg/400 units may be potentially mis-labeled as DIGOXIN, Tablet, 125 mcg, NDC 00527132401, Pedigree: AD76675_4, EXP: 6/3/2014; or AMANTADINE HCL, Tablet, 100 mg, NDC 00832011100, Pedigree: AD54475_4, EXP: 5/20/2014.

Code information

CALCIUM CARBONATE +D3, Tablet, 600 mg/400 units has the following codes: Pedigree: W002610, EXP: 6/4/2014; Pedigree: AD54576_1, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 3 of 273

OMEGA-3 FATTY ACID, Capsule, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904404360

D-465-2014

Recall number: D-465-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,799 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; OMEGA-3 FATTY ACID, Capsule, 1000 mg may be potentially mis-labeled as DOCUSATE CALCIUM, Capsule, 240 mg, NDC 00536375501, Pedigree: AD33897_16, EXP: 5/9/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: AD33897_19, EXP: 5/9/2014; PSEUDOEPHEDRINE HCL, Tablet, 60 mg, NDC 00904512559, Pedigree: W002856, EXP: 6/7/2014; DOCUSATE SODIUM, Capsule, 50 mg, N

Code information

OMEGA-3 FATTY ACID, Capsule, 1000 mg has the following codes: Pedigree: AD33897_19, EXP: 5/9/2014; Pedigree: AD32328_5, EXP: 5/9/2014; Pedigree: W002852, EXP: 6/7/2014; Pedigree: AD62865_13, EXP: 5/23/2014; Pedigree: W002509, EXP: 6/3/2014; Pedigree: W003705, EXP: 6/25/2014; Pedigree: AD22845_7, EXP: 5/2/2014; Pedigree: AD39588_7, EXP:5/13/2014; Pedigree: AD73627_20, EXP: 5/30/2014; Pedigree: W003870, EXP: 6/27/2014; Pedigree: AD46300_14, EXP: 5/15/2014; Pedigree: AD60211_14, EXP: 5/22/2014; Pedigree: W003052, EXP: 6/12/2014; Pedigree: W003217, EXP: 6/14/2014; Pedigree: AD73623_4, EXP: 5/30/2014; Pedigree: W003462, EXP: 6/20/2014; Pedigree: W003195, EXP: 6/13/2014; Pedigree: W003473, EXP: 6/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 4 of 273

CYANOCOBALAMIN, Tablet, 1000 mcg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904421713

D-466-2014

Recall number: D-466-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,821 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CYANOCOBALAMIN, Tablet, 1000 mcg may be potentially mislabeled as VITAMIN B COMPLEX W/C, Tablet, NDC 00904026013, Pedigree: AD21846_43, EXP: 5/1/2014; NIACIN TR, Capsule, 500 mg, NDC 00904063160, Pedigree: AD46257_22, EXP: 5/15/2014; chlorproMAZINE HCl, Tablet, 50 mg, NDC 00832030200, Pedigree: AD32973_4, EXP: 5/9/2014; PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet, NDC

Code information

CYANOCOBALAMIN, Tablet, 1000 mcg has the following codes Pedigree: AD21846_46, EXP: 5/1/2014; Pedigree: AD46257_59, EXP: 5/15/2014; Pedigree: AD32582_3, EXP: 5/9/2014; Pedigree: AD60240_51, EXP: 5/22/2014; Pedigree: W002839, EXP: 6/7/2014; Pedigree: W003026, EXP: 6/12/2014; Pedigree: W003075, EXP: 6/12/2014; Pedigree: W003322, EXP: 6/19/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 5 of 273

NIACIN TR, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00904434260

D-467-2014

Recall number: D-467-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 103 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NIACIN TR, Tablet, 500 mg may be potentially mislabeled as LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: W002968, EXP: 6/11/2014.

Code information

NIACIN TR, Tablet, 500 mg has the following code Pedigree: W002969, EXP: 6/11/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 6 of 273

COENZYME Q-10, Capsule, 30 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904501546

D-468-2014

Recall number: D-468-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; COENZYME Q-10, Capsule, 30 mg may be potentially mislabeled as PANCRELIPASE DR, Capsule, 12000 /38000 /60000 USP units, NDC 00032121201, Pedigree: W002819, EXP: 6/7/2014.

Code information

COENZYME Q-10, Capsule, 30 mg has the following code Pedigree: W002814, EXP: 6/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 7 of 273

PSEUDOEPHEDRINE HCL, Tablet, 30 mg, Rx in Oregon, Distributed by: AidaPak Service, LLC, NDC 00904505360

D-469-2014

Recall number: D-469-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PSEUDOEPHEDRINE HCL, Tablet, 30 mg may be potentially mislabeled as D-ALPHA TOCOPHERYL ACETATE, Capsule, 400 units, NDC 49348041010, Pedigree: AD52993_28, EXP: 5/20/2014.

Code information

PSEUDOEPHEDRINE HCL, Tablet, 30 mg has the following code Pedigree: AD52993_37, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 8 of 273

CALCIUM CITRATE, Tablet, 200 mg Elemental Calcium, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260

D-470-2014

Recall number: D-470-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CALCIUM CITRATE, Tablet, 200 mg Elemental Calcium may be potentially mislabeled as TRIAMTERENE/HCTZ, Tablet, 37.5 mg/25 mg, NDC 00378135201, Pedigree: AD28333_4, EXP: 5/6/2014.

Code information

CALCIUM CITRATE, Tablet, 200 mg Elemental Calcium has the following code Pedigree: AD28333_1, EXP: 5/8/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 9 of 273

CALCIUM CITRATE, Tablet, 950 mg (200 mg Elem Ca), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260

D-471-2014

Recall number: D-471-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 900 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CALCIUM CITRATE, Tablet, 950 mg (200 mg Elem Ca) may be potentially mislabeled as VALSARTAN, Tablet, 160 mg, NDC 00078035934, Pedigree: W002767, EXP: 6/6/2014; LACTOBACILLUS ACIDOPHILUS, Capsule, 500 MILLION CFU, NDC 43292050022, Pedigree: AD60240_20, EXP: 5/22/2014; PYRIDOXINE HCL, Tablet, 50 mg, NDC 51645090901, Pedigree: AD73521_25, EXP: 5/30/2014.

Code information

CALCIUM CITRATE, Tablet, 950 mg (200 mg Elem Ca) has the following codes Pedigree: W002699, EXP: 6/5/2014; Pedigree: AD60240_27, EXP: 5/22/2014; Pedigree: AD73521_28, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 10 of 273

CALCIUM CITRATE, Tablet, 950 mg (200 mg Elem Calcium), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260

D-472-2014

Recall number: D-472-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 298 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CALCIUM CITRATE, Tablet, 950 mg (200 mg Elem Calcium) may be potentially mislabeled as tiZANidine HCL, Tablet, 2 mg, NDC 57664050289, Pedigree: W003750, EXP: 6/26/2014.

Code information

CALCIUM CITRATE, Tablet, 950 mg (200 mg Elem Calcium) has the following code Pedigree: W003720, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 11 of 273

CALCIUM CITRATE, Tablet, 950 mg (200 MG ELEMENTAL Ca), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260

D-473-2014

Recall number: D-473-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CALCIUM CITRATE, Tablet, 950 mg (200 MG ELEMENTAL Ca) may be potentially mislabeled as TRIMETHOBENZAMIDE HCL, Capsule, 300 mg, NDC 53489037601, Pedigree: AD21858_10, EXP: 5/1/2014.

Code information

CALCIUM CITRATE, Tablet, 950 mg (200 MG ELEMENTAL Ca) has the following code Pedigree: AD21846_24, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 12 of 273

CALCIUM CITRATE, Tablet, 950 mg (200 mg Elemental Calcium), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904506260

D-474-2014

Recall number: D-474-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CALCIUM CITRATE, Tablet, 950 mg (200 mg Elemental Calcium) may be potentially mislabeled as LITHIUM CARBONATE ER, Tablet, 450 mg, NDC 00054002025, Pedigree: AD46265_10, EXP: 5/15/2014.

Code information

CALCIUM CITRATE, Tablet, 950 mg (200 mg Elemental Calcium) has the following code Pedigree: AD46257_43, EXP: 5/15/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 13 of 273

PSEUDOEPHEDRINE HCL, Tablet, 60 mg, Rx in Oregon, Distributed by: AidaPak Service, LLC, NDC 00904512559

D-475-2014

Recall number: D-475-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PSEUDOEPHEDRINE HCL, Tablet, 60 mg may be potentially mislabeled as REPAGLINIDE, Tablet, 1 mg, NDC 00169008281, Pedigree: W002855, EXP: 6/7/2014.

Code information

PSEUDOEPHEDRINE HCL, Tablet, 60 mg has the following code Pedigree: W002856, EXP: 6/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 14 of 273

ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/250 mg/65 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904513559

D-476-2014

Recall number: D-476-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/250 mg/65 mg may be potentially mislabeled as NAPROXEN, Tablet, 500 mg, NDC 53746019001, Pedigree: AD68025_8, EXP: 5/28/2014.

Code information

ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/250 mg/65 mg has the following code Pedigree: AD68022_4, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 15 of 273

GUAIFENESIN, Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00904515460

D-477-2014

Recall number: D-477-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; GUAIFENESIN, Tablet, 200 mg may be potentially mislabeled as PANCRELIPASE DR, Capsule, 24000 /76000 /120000 USP units, NDC 00032122401, Pedigree: W002850, EXP: 6/7/2014.

Code information

GUAIFENESIN, Tablet, 200 mg has the following code Pedigree: W002853, EXP: 6/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 16 of 273

PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904531360

D-478-2014

Recall number: D-478-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,501 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet may be potentially mislabeled as RILUZOLE, Tablet, 50 mg, NDC 00075770060, Pedigree: AD62992_11, EXP: 5/23/2014; ASPIRIN, Chew Tablet, 81 mg, NDC 00536329736, Pedigree: W003093, EXP: 6/13/2014; NIACIN TR, Capsule, 250 mg, NDC 00904062960, Pedigree: W003478, EXP: 6/20/2014; PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 009045

Code information

PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet has the following codes Pedigree: AD62986_22, EXP: 5/23/2014; Pedigree: W003098, EXP: 6/13/2014; Pedigree: W003479, EXP: 6/20/2014; Pedigree: W003480, EXP: 6/20/2014; Pedigree: AD52993_13, EXP: 5/20/2014; Pedigree: AD60428_7, EXP: 5/22/2014; Pedigree: AD73652_16, EXP: 5/30/2014; Pedigree: W003706, 6/25/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 17 of 273

ZINC SULFATE, Capsule, 220 mg (50 mg Elem Zn), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904533260

D-479-2014

Recall number: D-479-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 99 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ZINC SULFATE, Capsule, 220 mg (50 mg Elem Zn) may be potentially mislabeled as PHOSPHORUS, Tablet, 250 mg, NDC 64980010401, Pedigree: AD56916_1, EXP: 5/21/2014.

Code information

ZINC SULFATE, Capsule, 220 mg (50 mg Elem Zn) has the following code Pedigree: AD57624_1, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 18 of 273

ZINC SULFATE, Capsule, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904533260

D-480-2014

Recall number: D-480-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ZINC SULFATE, Capsule, 50 mg may be potentially mislabeled as SERTRALINE HCL, Tablet, 50 mg, NDC 16714061204, Pedigree: AD30993_14, EXP: 5/9/2014.

Code information

ZINC SULFATE, Capsule, 50 mg has the following code Pedigree: AD30994_8, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 19 of 273

GLUCOSAMINE/CHONDROITIN DS, Capsule, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904548152

D-481-2014

Recall number: D-481-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; GLUCOSAMINE/CHONDROITIN DS, Capsule, 500 mg/400 mg may be potentially mislabeled as GLYCOPYRROLATE, Tablet, 2 mg, NDC 00603318121, Pedigree: AD22865_4, EXP: 5/2/2014; PREGABALIN, Capsule, 25 mg, NDC 00071101268, Pedigree: W003121, EXP: 6/13/2014; MULTIVITAMIN/MULTIMINERAL, Chew Tablet, NDC 00536344308, Pedigree: AD73521_10, EXP: 5/30/2014.

Code information

GLUCOSAMINE/CHONDROITIN DS, Capsule, 500 mg/400 mg has the following codes Pedigree: AD21846_14, EXP: 5/1/2014; Pedigree: W003316, EXP: 6/18/2014; Pedigree: AD73521_16, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 20 of 273

MULTIVITAMIN/MULTIMINERAL, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904549213

D-482-2014

Recall number: D-482-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 520 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MULTIVITAMIN/MULTIMINERAL, Tablet may be potentially mislabeled as LISINOPRIL, Tablet, 2.5 mg, NDC 64679092701, Pedigree: AD25264_4, EXP: 5/3/2014.

Code information

MULTIVITAMIN/MULTIMINERAL, Tablet has the following code Pedigree: AD23082_13, EXP: 11/1/2013.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 21 of 273

diphenhydrAMINE HCl, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 00904555159

D-483-2014

Recall number: D-483-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 901 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; diphenhydrAMINE HCl, Tablet, 25 mg may be potentially mislabeled as ATORVASTATIN CALCIUM, Tablet, 40 mg, NDC 00378212177, Pedigree: AD33897_10, EXP: 5/9/2014; ATORVASTATIN CALCIUM, Tablet, 10 mg, NDC 00378201577, Pedigree: W002774, EXP: 6/6/2014; PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet, NDC 51991056601, Pedigree: W003511, EXP: 6/21/2014; VENLAFAXINE, Tablet, 25 mg

Code information

diphenhydrAMINE HCl, Tablet, 25 mg has the following codes Pedigree: AD33897_13, EXP: 5/9/2014; Pedigree: W002775, EXP: 6/6/2014; Pedigree: W003513, EXP: 6/21/2014; Pedigree: AD67992_4, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 22 of 273

GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904559293

D-484-2014

Recall number: D-484-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD60211_11, EXP: 5/22/2014.

Code information

GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg has the following code Pedigree: AD60211_17, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 23 of 273

CHOLECALCIFEROL, Tablet, 400 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904582360

D-485-2014

Recall number: D-485-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,199 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CHOLECALCIFEROL, Tablet, 400 units may be potentially mislabeled as CYANOCOBALAMIN, Tablet, 500 mcg, NDC 00536355101, Pedigree: AD37056_10, EXP: 5/10/2014; ROSUVASTATIN CALCIUM, Tablet, 5 mg, NDC 00310075590, Pedigree: W002567, EXP: 6/3/2014; PYRIDOXINE HCL, Tablet, 100 mg, NDC 00536440901, Pedigree: AD76686_4, EXP: 5/31/2014; CYANOCOBALAMIN, Tablet, 500 mcg, NDC 0053

Code information

CHOLECALCIFEROL, Tablet, 400 units has the following codes Pedigree: AD37056_13, EXP: 5/10/2014; Pedigree: W002574, EXP: 6/3/2014; Pedigree: AD76686_7, EXP: 5/31/2014; Pedigree: AD60578_27, EXP: 5/29/2014; Pedigree: W003540, EXP: 6/21/2014; Pedigree: AD52993_25, EXP: 5/20/2014; Pedigree: W002715, EXP: 6/5/2014; Pedigree: AD30197_31, EXP: 5/9/2014; Pedigree: AD73592_8, EXP: 5/31/2014; Pedigree: W002642, EXP: 6/4/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 24 of 273

CHOLECALCIFEROL, Tablet, 1000 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904582460

D-486-2014

Recall number: D-486-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,399 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CHOLECALCIFEROL, Tablet, 1000 units may be potentially mislabeled as ASPIRIN, Chew Tablet, 81 mg, NDC 00536329736, Pedigree: W003459, EXP: 6/20/2014; MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 37205018581, Pedigree: AD32328_8, EXP: 5/9/2014; CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: W002715, EXP: 6/5/2014; GLYCOPYRROLATE, Tablet, 2 mg, NDC 49884006601

Code information

CHOLECALCIFEROL, Tablet, 1000 units has the following codes Pedigree: W003464, EXP: 6/20/2014; Pedigree: AD33897_37, EXP: 5/9/2014; Pedigree: W002779, EXP: 6/6/2014; Pedigree: W003626, EXP: 6/25/2014; Pedigree: W003827, EXP: 6/27/2014; Pedigree: AD33897_34, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 25 of 273

CHOLECALCIFEROL, Capsule, 5000 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 0904598660

D-487-2014

Recall number: D-487-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CHOLECALCIFEROL, Capsule, 5000 units may be potentially mislabeled as SEVELAMER CARBONATE, Tablet, 800 mg, NDC 58468013001, Pedigree: AD70629_16, EXP: 5/29/2014; CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: W003540, EXP: 6/21/2014; THIAMINE HCL, Tablet, 100 mg, NDC 00904054460, Pedigree: AD52993_16, EXP: 5/20/2014.

Code information

CHOLECALCIFEROL, Capsule, 5000 units has the following codes Pedigree: AD70629_19, EXP: 5/29/2014; Pedigree: W003541, EXP: 6/21/2014; Pedigree: AD52993_22, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 26 of 273

CHOLECALCIFEROL, Tablet, 2000 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904615760

D-488-2014

Recall number: D-488-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,998 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CHOLECALCIFEROL, Tablet, 2000 units may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 00904052060, Pedigree: AD46312_34, EXP: 5/16/2014; PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 13811051410, Pedigree: AD65314_1, EXP: 5/24/2014; RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: W003538, EXP: 6/21/2014; LEVOTHYROXINE SODIUM, Tablet, 175

Code information

CHOLECALCIFEROL, Tablet, 2000 units has the following codes Pedigree: AD46312_37, EXP: 5/16/2014; Pedigree: AD65311_1, EXP: 5/24/2014; Pedigree: W003539, EXP: 6/21/2014; Pedigree: W003744, EXP: 6/26/2014; Pedigree: AD54586_10, EXP: 5/21/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 27 of 273

FERROUS SULFATE, Tablet, 325 mg (65 mg Elem Fe), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904759160

D-489-2014

Recall number: D-489-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 402 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FERROUS SULFATE, Tablet, 325 mg (65 mg Elem Fe) may be potentially mislabeled as COENZYME Q-10, Capsule, 100 mg, NDC 37205055065, Pedigree: W002711, EXP: 6/6/2014; VENLAFAXINE HCL, Tablet, 25 mg, NDC 00093019901, Pedigree: W002825, EXP: 12/31/2013; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: AD60236_1, EXP: 5/22/2014.

Code information

FERROUS SULFATE, Tablet, 325 mg (65 mg Elem Fe) has the following codes Pedigree: W002717, EXP: 6/6/2014; Pedigree: W002826, EXP: 6/7/2014; Pedigree: AD60268_1, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 28 of 273

FERROUS SULFATE, Tablet, 325 mg (65 mg Elemental Iron), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904759160

D-490-2014

Recall number: D-490-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FERROUS SULFATE, Tablet, 325 mg (65 mg Elemental Iron) may be potentially mislabeled as RAMIPRIL, Capsule, 2.5 mg, NDC 68180058901, Pedigree: AD54549_16, EXP: 5/20/2014.

Code information

FERROUS SULFATE, Tablet, 325 mg (65 mg Elemental Iron) has the following code Pedigree: AD54553_1, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 29 of 273

DOCUSATE SODIUM, Capsule, 250 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904789159

D-491-2014

Recall number: D-491-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 4,318 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; DOCUSATE SODIUM, Capsule, 250 mg may be potentially mislabeled as ATROPINE SULFATE/DIPHENOXYLATE HCL, Tablet, 0.025 mg/2.5 mg, NDC 00378041501, Pedigree: AD65475_13, EXP: 5/28/2014; VALSARTAN, Tablet, 80 mg, NDC 00078035834, Pedigree: AD68025_1, EXP: 5/28/2014; PANTOPRAZOLE SODIUM DR, Tablet, 40 mg, NDC 64679043402, Pedigree: AD37063_10, EXP: 5/13/2014; DOCUSATE SODIUM

Code information

DOCUSATE SODIUM, Capsule, 250 mg has the following codes Pedigree: AD68028_1, EXP: 5/28/2014; Pedigree: AD68022_1, EXP: 5/28/2014; Pedigree: AD37072_1, EXP: 5/13/2014; Pedigree: AD37072_4, EXP: 5/13/2014; Pedigree: AD56924_1, EXP: 5/21/2014; Pedigree: W003671, EXP: 6/25/2014; Pedigree: W002920, EXP: 6/10/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 30 of 273

MAGNESIUM CHLORIDE DR, Tablet, 64 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904791152

D-492-2014

Recall number: D-492-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MAGNESIUM CHLORIDE DR, Tablet, 64 mg may be potentially mislabeled as SELEGILINE HCL, Capsule, 5 mg, NDC 67253070006, Pedigree: AD54549_19, EXP: 5/20/2014; PHOSPHORUS, Tablet, 250 mg, NDC 64980010401, Pedigree: AD70639_10, EXP: 5/29/2014.

Code information

MAGNESIUM CHLORIDE DR, Tablet, 64 mg has the following codes Pedigree: AD54510_1, EXP: 2/28/2014; Pedigree: AD70615_1, EXP: 2/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 31 of 273

BISACODYL EC, Tablet, 5 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 00904792760

D-493-2014

Recall number: D-493-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; BISACODYL EC, Tablet, 5 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: AD37056_13, EXP: 5/10/2014.

Code information

BISACODYL EC, Tablet, 5 mg has the following code Pedigree: AD34931_1, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 32 of 273

MELATONIN, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 04746900466

D-494-2014

Recall number: D-494-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 359 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MELATONIN, Tablet, 1 mg may be potentially mislabeled as QUETIAPINE FUMARATE, Tablet, 12.5 MG (1/2 of 25 MG), NDC 47335090288, Pedigree: AD21790_79, EXP: 5/1/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: AD73521_13, EXP: 5/30/2014.

Code information

MELATONIN, Tablet, 1 mg has the following codes Pedigree: AD21846_17, EXP: 5/1/2014; Pedigree: AD73521_19, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 33 of 273

NAPROXEN, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 05374601901

D-495-2014

Recall number: D-495-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NAPROXEN, Tablet, 500 mg may be potentially mislabeled as THIOTHIXENE, Capsule, 1 mg, NDC 00378100101, Pedigree: AD54549_22, EXP: 5/20/2014; HYDROCHLOROTHIAZIDE, Tablet, 12.5 mg, NDC 00228282011, Pedigree: AD67989_13, EXP: 5/28/2014.

Code information

NAPROXEN, Tablet, 500 mg has the following codes Pedigree: AD54516_1, EXP: 5/20/2014; Pedigree: AD68025_8, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 34 of 273

OMEGA-3 FATTY ACID, Capsule, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 05445800022

D-496-2014

Recall number: D-496-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; OMEGA-3 FATTY ACID, Capsule, 1000 mg may be potentially mislabeled as NORTRIPTYLINE HCL, Capsule, 50 mg, NDC 00093081201, Pedigree: AD21790_70, EXP: 5/1/2014.

Code information

OMEGA-3 FATTY ACID, Capsule, 1000 mg has the following code Pedigree: AD21858_4, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 35 of 273

MELATONIN, Tablet, 3 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 08770140813

D-497-2014

Recall number: D-497-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 3,710 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MELATONIN, Tablet, 3 mg may be potentially mislabeled as VITAMIN B COMPLEX, Capsule, NDC 00536478701, Pedigree: AD32757_4, EXP: 5/13/2014; MULTIVITAMIN/ MULTIMINERAL/ LUTEIN, Capsule, NDC 24208063210, Pedigree: W003025, EXP: 6/12/2014; LACTASE ENZYME, Tablet, 3000 units, NDC 24385014976, Pedigree: W003721, EXP: 6/26/2014; GLUCOSAMINE/CHONDROITIN DS, Capsule, 500 mg/400

Code information

MELATONIN, Tablet, 3 mg has the following codes Pedigree: AD46257_56, EXP: 5/15/2014; Pedigree: W003022, EXP: 6/12/2014; Pedigree: W003723, EXP: 6/26/2014; Pedigree: AD21846_34, EXP: 5/1/2014; Pedigree: AD30028_28, EXP: 5/7/2014; Pedigree: AD60240_39, EXP: 5/22/2014; Pedigree: AD73521_31, EXP: 5/30/2014; Pedigree: W002701, EXP: 6/5/2014; Pedigree: W003320, EXP: 6/19/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 36 of 273

GALANTAMINE HBr ER, Capsule, 8 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 10147089103

D-498-2014

Recall number: D-498-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; GALANTAMINE HBr ER, Capsule, 8 mg may be potentially mislabeled as FAMOTIDINE, Tablet, 20 mg, NDC 16714036104, Pedigree: W003508, EXP: 6/21/2014.

Code information

GALANTAMINE HBr ER, Capsule, 8 mg has the following code Pedigree: W003509, EXP: 6/21/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 37 of 273

ITRACONAZOLE, Capsule, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 10147170003

D-499-2014

Recall number: D-499-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ITRACONAZOLE, Capsule, 100 mg may be potentially mislabeled as FAMCICLOVIR, Tablet, 500 mg, NDC 00093811956, Pedigree: AD54549_4, EXP: 5/20/2014.

Code information

ITRACONAZOLE, Capsule, 100 mg has the following code Pedigree: AD54549_10, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 38 of 273

NIACIN TR, Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 10939043533

D-500-2014

Recall number: D-500-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 101 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NIACIN TR, Tablet, 250 mg may be potentially mislabeled as SOLIFENACIN SUCCINATE, Tablet, 5 mg, NDC 51248015001, Pedigree: W003755, EXP: 6/26/2014.

Code information

NIACIN TR, Tablet, 250 mg has the following code Pedigree: W003756, EXP: 5/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 39 of 273

OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 11523726503

D-501-2014

Recall number: D-501-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 210 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,100 mg may be potentially mislabeled as CYANOCOBALAMIN, Tablet, 1000 mcg, NDC 00536355601, Pedigree: W003788, EXP: 6/27/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: W003870, EXP: 6/27/2014.

Code information

OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,100 mg has the following codes Pedigree: W003789, EXP: 6/27/2014; Pedigree: W003873, EXP: 6/27/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 40 of 273

OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,110 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 11523726503

D-502-2014

Recall number: D-502-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 294 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,110 mg may be potentially mislabeled as ACETAMINOPHEN, CHEW Tablet, 80 mg, NDC 00536323307, Pedigree: AD49399_1, EXP: 5/16/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: AD46300_11, EXP: 5/15/2014; MYCOPHENOLATE MOFETIL, Capsule, 250 mg, NDC 00781206701, Pedigree: AD65457_7, EXP: 5/24/2014.

Code information

OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,110 mg has the following codes Pedigree: AD49399_4, EXP: 5/16/2014; Pedigree: AD46300_17, EXP: 5/15/2014; Pedigree: AD65457_22, EXP: 5/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 41 of 273

OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/110 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 11523726503

D-503-2014

Recall number: D-503-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 84 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/110 mg may be potentially mislabeled as BENZOCAINE/MENTHOL, LOZENGE, 15 mg/2.6 mg, NDC 63824073116, Pedigree: AD42592_4, EXP: 5/14/2014.

Code information

OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/110 mg has the following code Pedigree: AD42584_15, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 42 of 273

OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1110 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 11523726503

D-504-2014

Recall number: D-504-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 210 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1110 mg may be potentially mislabeled as LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: AD70655_8, EXP: 5/29/2014; PYRIDOXINE HCL, Tablet, 100 mg, NDC 00536440901, Pedigree: AD73627_32, EXP: 5/30/2014.

Code information

OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1110 mg has the following codes Pedigree: AD70655_20, EXP: 5/29/2014; Pedigree: AD73627_35, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 43 of 273

OMEGA-3 FATTY ACID, Capsule, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 11845014882

D-505-2014

Recall number: D-505-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 116 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; OMEGA-3 FATTY ACID, Capsule, 1000 mg may be potentially mislabeled as tiZANidine HCL, Tablet, 2 mg, NDC 57664050289, Pedigree: AD70700_10, EXP: 5/29/2014.

Code information

OMEGA-3 FATTY ACID, Capsule, 1000 mg has the following code Pedigree: AD70700_7, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 44 of 273

CHLOROPHYLLIN COPPER COMPLEX, Tablet, 100 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 11868000901

D-506-2014

Recall number: D-506-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 135 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CHLOROPHYLLIN COPPER COMPLEX, Tablet, 100 mg may be potentially mislabeled as traZODone HCl, Tablet, 50 mg, NDC 50111043301, Pedigree: AD37088_4, EXP: 5/9/2014.

Code information

CHLOROPHYLLIN COPPER COMPLEX, Tablet, 100 mg has the following code Pedigree: AD34928_1, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 45 of 273

PARoxetine HCl, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 13107015430

D-507-2014

Recall number: D-507-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PARoxetine HCl, Tablet, 10 mg may be potentially mislabeled as PANTOPRAZOLE SODIUM DR, Tablet, 20 mg, NDC 62175018046, Pedigree: AD52778_64, EXP: 5/20/2014.

Code information

PARoxetine HCl, Tablet, 10 mg has the following code Pedigree: AD52778_67, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 46 of 273

lamoTRIgine, Tablet, 50 mg (1/2 of 100 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 13668004701

D-508-2014

Recall number: D-508-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 600 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; lamotrigine, Tablet, 50 mg (1/2 of 100 mg) may be potentially mislabeled as OXYBUTYNIN CHLORIDE, Tablet, 2.5 mg (1/2 of 5 mg), NDC 00603497521, Pedigree: AD73525_64, EXP: 5/30/2014; FEXOFENADINE HCL, Tablet, 60 mg, NDC 45802042578, Pedigree: AD46257_50, EXP: 5/15/2014.

Code information

lamoTRIgine, Tablet, 50 mg (1/2 of 100 mg) has the following codes Pedigree: ADWA00002116, EXP: 5/31/2014; Pedigree: AD46265_31, EXP: 5/15/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 47 of 273

PRAMIPEXOLE DI-HCL, Tablet, 0.125 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 13668009190

D-509-2014

Recall number: D-509-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 359 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PRAMIPEXOLE DI-HCL, Tablet, 0.125 mg may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 00904549213, Pedigree: AD23082_13, EXP: 11/1/2013; PERPHENAZINE, Tablet, 16 mg, NDC 00781104901, Pedigree: W003682, EXP: 6/25/2014.

Code information

PRAMIPEXOLE DI-HCL, Tablet, 0.125 mg has the following codes Pedigree: AD25264_10, EXP: 5/3/2014; Pedigree: W003683, EXP: 6/25/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 48 of 273

PANTOPRAZOLE SODIUM DR, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 13668009690

D-510-2014

Recall number: D-510-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PANTOPRAZOLE SODIUM DR, Tablet, 20 mg may be potentially mislabel as NORTRIPTYLINE HCL, Capsule, 75 mg, NDC 00093081301, Pedigree: W003694, EXP: 6/26/2014.

Code information

PANTOPRAZOLE SODIUM DR, Tablet, 20 mg has the following code Pedigree: W003695, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 49 of 273

LOSARTAN POTASSIUM, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 13668011390

D-511-2014

Recall number: D-511-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LOSARTAN POTASSIUM, Tablet, 25 mg may be potentially mislabeled as DISOPYRAMIDE PHOSPHATE, Capsule, 150 mg, NDC 00093312901, Pedigree: AD65323_4, EXP: 5/29/2014.

Code information

LOSARTAN POTASSIUM, Tablet, 25 mg has the following code Pedigree: AD65323_10, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 50 of 273

PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 13811051410

D-512-2014

Recall number: D-512-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,400 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet may be potentially mislabeled as CYANOCOBALAMIN, Tablet, 100 mcg, NDC 00536354201, Pedigree: AD62840_1, EXP: 5/24/2014.

Code information

PRENATAL MULTIVITAMIN/MULTIMINERAL, Tablet has the following code Pedigree: AD65314_1, EXP: 5/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 51 of 273

prednisoLONE, Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC,NDC 16477050501

D-513-2014

Recall number: D-513-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; prednisoLONE, Tablet, 5 mg may be potentially mislabeled as ASPIRIN/ER DIPYRIDAMOLE, Capsule, 25 mg/200 mg, NDC 00597000160, Pedigree: W003644, EXP: 8/24/2013.

Code information

prednisoLONE, Tablet, 5 mg has the following code Pedigree: W003627, EXP: 6/25/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 52 of 273

PROPRANOLOL HCL, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714002104

D-514-2014

Recall number: D-514-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PROPRANOLOL HCL, Tablet, 10 mg may be potentially mislabeled as PIOGLITAZONE HCL, Tablet, 15 mg, NDC 00093204856, Pedigree: AD52778_70, EXP: 5/21/2014.

Code information

PROPRANOLOL HCL, Tablet, 10 mg has the following code Pedigree: AD52778_73, EXP: 5/21/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 53 of 273

ALLOPURINOL Tablet, 300 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714004204

D-515-2014

Recall number: D-515-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ALLOPURINOL Tablet, 300 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: AD52993_25, EXP: 5/20/2014.

Code information

ALLOPURINOL Tablet, 300 mg has the following code Pedigree: AD52778_1, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 54 of 273

VENLAFAXINE Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714031101

D-516-2014

Recall number: D-516-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; VENLAFAXINE Tablet, 25 mg may be potentially mislabeled as OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,110 mg, NDC 11523726503, Pedigree: AD65457_22, EXP: 5/24/2014.

Code information

VENLAFAXINE Tablet, 25 mg has the following code Pedigree: AD67989_4, EXP: 11/30/2013.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 55 of 273

FLUoxetine HCl Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714035103

D-517-2014

Recall number: D-517-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FLUoxetine HCl, Capsule, 10 mg may be potentially mislabeled as PANCRELIPASE DR, Capsule, 24000 /76000 /120000 USP units, NDC 00032122401, Pedigree: AD70585_10, EXP: 5/29/2014.

Code information

FLUoxetine HCl, Capsule, 10 mg has the following code Pedigree: AD70585_13, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 56 of 273

FAMOTIDINE Tablet, 20 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 16714036104

D-518-2014

Recall number: D-518-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 700 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FAMOTIDINE Tablet, 20 mg may be potentially mislabeled as CARVEDILOL PHOSPHATE ER, Capsule, 20 mg, NDC 00007337113, Pedigree: W003225, EXP: 6/17/2014; DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: W003506, EXP: 6/21/2014; FAMOTIDINE, Tablet, 20 mg, NDC 16714036104, Pedigree: W003507, EXP: 6/21/2014; MYCOPHENOLATE MOFETIL, Capsule, 250 mg, NDC 0037822500

Code information

FAMOTIDINE Tablet, 20 mg has the following codes Pedigree: W003226, EXP: 6/17/2014; Pedigree: W003507, EXP: 6/21/2014; Pedigree: W003508, EXP: 6/21/2014; Pedigree: W003764, EXP: 6/26/2014; Pedigree: W003406, EXP: 6/19/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 57 of 273

FINASTERIDE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714052201

D-519-2014

Recall number: D-519-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 120 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FINASTERIDE, Tablet, 5 mg may be potentially mislabeled as DIGOXIN, Tablet, 0.125 mg, NDC 00115981101, Pedigree: AD62829_8, EXP: 5/23/2014; PHYTONADIONE, Tablet, 5 mg, NDC 25010040515, Pedigree: W003061, EXP: 5/31/2014.

Code information

FINASTERIDE Tablet, 5 mg has the following codes Pedigree: AD62846_1, EXP: 2/28/2014; Pedigree: W003031, EXP: 2/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 58 of 273

LOSARTAN POTASSIUM Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714058102

D-520-2014

Recall number: D-520-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 448 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LOSARTAN POTASSIUM, Tablet, 25 mg may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00904789159, Pedigree: AD68028_1, EXP: 5/28/2014; METOPROLOL TARTRATE, Tablet, 50 mg, NDC 00093073301, Pedigree: W003844, EXP: 6/27/2014; LACTOBACILLUS ACIDOPHILUS, Tablet, 35 Million, NDC 00536718101, Pedigree: W003865, EXP: 6/27/2014; OXYBUTYNIN CHLORIDE, Tablet,

Code information

LOSARTAN POTASSIUM Tablet, 25 mg has the following codes Pedigree: AD67989_7, EXP: 5/28/2014; Pedigree: W003845, EXP: 6/27/2014; Pedigree: W003899, EXP: 6/27/2014; Pedigree: AD22616_7, EXP: 5/2/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 59 of 273

PRAMIPEXOLE DI-HCL Tablet, 0.25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714058501

D-521-2014

Recall number: D-521-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PRAMIPEXOLE DI-HCL, Tablet, 0.25 mg may be potentially mislabeled as TACROLIMUS, Capsule, 1 mg, NDC 00781210301, Pedigree: W003704, EXP: 6/26/2014.

Code information

PRAMIPEXOLE DI-HCL Tablet, 0.25 mg has the following code Pedigree: W003761, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 60 of 273

PRAMIPEXOLE DI-HCL Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714058701

D-522-2014

Recall number: D-522-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PRAMIPEXOLE DI-HCL, Tablet, 1 mg may be potentially mislabel as MISOPROSTOL, Tablet, 200 mcg, NDC 59762500801, Pedigree: W003117, EXP: 6/13/2014.

Code information

PRAMIPEXOLE DI-HCL Tablet, 1 mg has the following code Pedigree: W003150, EXP: 6/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 61 of 273

SERTRALINE HCL Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714061204

D-523-2014

Recall number: D-523-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 500 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; SERTRALINE HCL Tablet, 50 mg may be potentially mislabeled as NORTRIPTYLINE HCL, Capsule, 10 mg, NDC 00093081001, Pedigree: AD70585_4, EXP: 5/29/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003574, EXP: 6/24/2014; OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,110 mg, NDC 11523726503, Pedigree: AD46300_17, EXP: 5/15/2014; CHOLECALCIFEROL, Tablet,

Code information

SERTRALINE HCL Tablet, 50 mg has the following codes Pedigree: AD70585_7, EXP: 5/29/2014; Pedigree: W003575, EXP: 6/24/2014; Pedigree: AD46426_1, EXP: 5/15/2014; Pedigree: AD30993_14, EXP: 5/9/2014; Pedigree: W003033, EXP: 6/12/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 62 of 273

SIMVASTATIN Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16714068303

D-524-2014

Recall number: D-524-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,000 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; SIMVASTATIN Tablet, 20 mg may be potentially mislabeled as VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet, NDC 60258016001, Pedigree: W003591, EXP: 6/24/2014.

Code information

SIMVASTATIN, Tablet, 20 mg has the following code Pedigree: W003580, EXP: 6/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 63 of 273

HYDROCHLOROTHIAZIDE Tablet, 12.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 16729018201

D-525-2014

Recall number: D-525-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; HYDROCHLOROTHIAZIDE Tablet, 12.5 mg may be potentially mislabeled as chlordiazePOXIDE HCl, Capsule, 25 mg, NDC 00555015902, Pedigree: AD46333_4, EXP: 5/16/2014.

Code information

HYDROCHLOROTHIAZIDE Tablet, 12.5 mg has the following code Pedigree: AD46414_25, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 64 of 273

hydrALAZINE HCl Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155000401

D-526-2014

Recall number: D-526-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 400 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; hydrALAZINE HCl Tablet, 100 mg may be potentially mislabeled as DOXEPIN HCL, Capsule, 150 mg, NDC 49884022201, Pedigree: AD46312_10, EXP: 5/16/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD73652_1, EXP: 5/29/2014; LEVOTHYROXINE SODIUM, Tablet, 112 mcg, NDC 00378181101, Pedigree: AD30197_13, EXP: 5/9/2014.

Code information

hydrALAZINE HCl Tablet, 100 mg has the following codes Pedigree: AD46312_13, EXP: 5/16/2014; Pedigree: AD73652_4, EXP: 5/29/2014; Pedigree: AD30197_7, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 65 of 273

LEFLUNOMIDE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155004303

D-527-2014

Recall number: D-527-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LEFLUNOMIDE Tablet, 10 mg may be potentially mislabeled as DOXYCYCLINE HYCLATE, Capsule, 100 mg, NDC 00143314250, Pedigree: W002645, EXP: 6/5/2014; SEVELAMER CARBONATE, Tablet, 800 mg, NDC 58468013001, Pedigree: W002623, EXP: 6/4/2014.

Code information

LEFLUNOMIDE Tablet, 10 mg has the following codes Pedigree: W002659, EXP: 6/5/2014; Pedigree: W002658, EXP: 6/4/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 66 of 273

metFORMIN HCl Tablet 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155010201

D-528-2014

Recall number: D-528-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; metFORMIN HCl Tablet, 500 mg may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 40985022921, Pedigree: AD32742_1, EXP: 5/1/2014.

Code information

metFORMIN HCl, Tablet 500 mg has the following code Pedigree: AD46312_25, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 67 of 273

PROPRANOLOL HCL Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155011001

D-529-2014

Recall number: D-529-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,299 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PROPRANOLOL HCL, Tablet, 10 mg may be potentially mislabeled as PERPHENAZINE, Tablet, 16 mg, NDC 00781104901, Pedigree: AD21790_31, EXP: 5/1/2014; buPROPion HCl ER (XL), Tablet, 150 mg, NDC 67767014130, Pedigree: AD52412_4, EXP: 4/30/2014; MULTIVITAMIN/MULTIMINERAL LOW IRON, Tablet, NDC 64376081601, Pedigree: AD60272_31, EXP: 5/22/2014; PERPHENAZINE, Tablet, 16 mg, NDC

Code information

PROPRANOLOL HCL Tablet, 10 mg has the following codes Pedigree: AD21790_34, EXP: 5/1/2014; Pedigree: AD52390_1, EXP: 5/17/2014; Pedigree: AD60272_37, EXP: 5/22/2014; Pedigree: W002732, EXP: 6/6/2014; Pedigree: W003229, EXP: 6/17/2014; Pedigree: AD60272_34, EXP: 5/22/2014; Pedigree: W003684, EXP: 6/25/2014; Pedigree: W002618, EXP: 6/4/2014; Pedigree: W003002, EXP: 6/11/2014; Pedigree: W003068, EXP: 6/12/2014; Pedigree: W003545, EXP: 6/21/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 68 of 273

PROPRANOLOL HCL Tablet, 5 mg (1/2 of 10 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 23155011001

D-530-2014

Recall number: D-530-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 198 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PROPRANOLOL HCL Tablet, 5 mg (1/2 of 10 mg) may be potentially mislabeled as LITHIUM CARBONATE ER, Tablet, 225 mg (1/2 of 450 mg), NDC 00054002025, Pedigree: AD73525_16, EXP: 5/30/2014.

Code information

PROPRANOLOL HCL, Tablet, 5 mg (1/2 of 10 mg) has the following code Pedigree: AD73525_25, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 69 of 273

PROPRANOLOL HCL Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155011010

D-531-2014

Recall number: D-531-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,999 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PROPRANOLOL HCL Tablet, 10 mg may be potentially mislabeled as LACTOBACILLUS ACIDOPHILUS, Capsule, NDC 54629011101, Pedigree: AD65311_4, EXP: 5/24/2014.

Code information

PROPRANOLOL HCL Tablet, 10 mg has the following code Pedigree: AD65317_1, EXP: 5/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 70 of 273

PROPRANOLOL HCL Tablet, 80 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155011401

D-532-2014

Recall number: D-532-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PROPRANOLOL HCL Tablet, 80 mg may be potentially mislabeled as LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: AD42584_12, EXP: 5/14/2014.

Code information

PROPRANOLOL HCL, Tablet, 80 mg has the following code Pedigree: AD42566_4, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 71 of 273

ACARBOSE, Tablet 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155014701

D-533-2014

Recall number: D-533-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ACARBOSE Tablet, 25 mg may be potentially mislabeled as LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: AD39588_4, EXP: 5/13/2014.

Code information

ACARBOSE Tablet, 25 mg has the following code Pedigree: AD32757_1, EXP: 5/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 72 of 273

VENLAFAXINE HCL Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 23155024801

D-534-2014

Recall number: D-534-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; VENLAFAXINE HCL Tablet, 50 mg may be potentially mislabeled as sulfaSALAzine, Tablet, 500 mg, NDC 00603580121, Pedigree: AD65475_19, EXP: 5/28/2014.

Code information

VENLAFAXINE HCL Tablet, 50 mg has the following code Pedigree: AD65475_22, EXP; 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 73 of 273

MULTIVITAMIN/ MULTIMINERAL/ LUTEIN Capsule, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 24208063210

D-535-2014

Recall number: D-535-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 204 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MULTIVITAMIN/ MULTIMINERAL/ LUTEIN Capsule may be potentially mislabeled as CAFFEINE, Tablet, 200 mg, NDC 24385060173, Pedigree: AD21846_37, EXP: 5/1/2014; CAFFEINE, Tablet, 200 mg, NDC 24385060173, Pedigree: AD60240_42, EXP: 5/22/2014; CAFFEINE, Tablet, 200 mg, NDC 24385060173, Pedigree: W003024, EXP: 6/12/2014; MELATONIN, Tablet, 3 mg, NDC 08770140813, Pedigree: AD73

Code information

MULTIVITAMIN/ MULTIMINERAL/ LUTEIN Capsule has the following codes Pedigree: AD21846_40, EXP: 5/2/2014; Pedigree: AD60240_45, EXP: 5/22/2014; Pedigree: W003025, EXP: 6/12/2014; Pedigree: AD73521_37, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 74 of 273

ERYTHROMYCIN DR EC Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 24338012213

D-536-2014

Recall number: D-536-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ERYTHROMYCIN DR EC Tablet, 250 mg may be potentially mislabeled as methylPREDNISolone, Tablet, 4 mg, NDC 00781502201, Pedigree: AD46426_10, EXP: 5/15/2014.

Code information

ERYTHROMYCIN DR EC Tablet, 250 mg has the following code Pedigree: AD46426_13, EXP: 5/15/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 75 of 273

LACTASE ENZYME Tablet, 3000 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 24385014976

D-537-2014

Recall number: D-537-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,872 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LACTASE ENZYME Tablet, 3000 units may be potentially mislabeled as BENZOCAINE/MENTHOL, LOZENGE, 15 mg/3.6 mg, NDC 63824072016, Pedigree: AD21811_4, EXP: 5/1/2014; ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/250 mg/65 mg, NDC 46122010478, Pedigree: W003722, EXP: 4/30/2014; guaiFENesin ER, Tablet, 600 mg, NDC 45802049878, Pedigree: AD30140_37, EXP: 5/7/2014; CALCIUM

Code information

LACTASE ENZYME Tablet, 3000 units has the following codes Pedigree: AD21846_31, EXP: 5/1/2014; Pedigree: W003721, EXP: 6/26/2014; Pedigree: AD30028_25, EXP: 5/7/2014; Pedigree: AD60240_36, EXP: 5/22/2014; Pedigree: W002700, EXP: 6/5/2014; Pedigree: AD46257_53, EXP: 5/15/2014; Pedigree: W003021, EXP: 6/12/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 76 of 273

NICOTINE POLACRILEX Gum, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 24385059471

D-538-2014

Recall number: D-538-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 50 Pieces of Gum

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NICOTINE POLACRILEX Gum, 2 mg may be potentially mislabeled as SACCHAROMYCES BOULARDII LYO, Capsule, 250 mg, NDC 00414200007, Pedigree: AD54586_4, EXP: 5/21/2014.

Code information

NICOTINE POLACRILEX Gum, 2 mg has the following code Pedigree: AD54586_7, EXP: 3/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 77 of 273

PHYTONADIONE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 25010040515

D-539-2014

Recall number: D-539-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 500 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PHYTONADIONE Tablet, 5 mg may be potentially mislabeled as medroxyPROGESTERone ACETATE, Tablet, 10 mg, NDC 59762374202, Pedigree: AD46312_19, EXP: 5/16/2014; HYDROCORTISONE, Tablet, 5 mg, NDC 00603389919, Pedigree: W003060, EXP: 6/12/2014; GALANTAMINE HBR ER, Capsule, 24 mg, NDC 47335083783, Pedigree: W003735, EXP: 5/31/2014; TORSEMIDE, Tablet, 10 mg, NDC 31722053001,

Code information

PHYTONADIONE Tablet, 5 mg has the following codes Pedigree: AD46312_22, EXP: 4/30/2014; Pedigree: W003061, EXP: 5/31/2014; Pedigree: W003737, EXP: 5/31/2014; Pedigree: AD25452_1, EXP: 4/30/2014; Pedigree: W003440, EXP: 5/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 78 of 273

CAFFEINE Tablet, 200 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 24385060173

D-540-2014

Recall number: D-540-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 128 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CAFFEINE Tablet, 200 mg may be potentially mislabeled as CALCIUM CITRATE, Tablet, 950 mg (200 mg ELEMENTAL Ca), NDC 00904506260, Pedigree: AD21846_24, EXP: 5/1/2014; CHOLECALCIFEROL, Capsule, 2000 units, NDC 00536379001, Pedigree: AD60240_4, EXP: 5/22/2014; FEXOFENADINE HCL, Tablet, 60 mg, NDC 45802042578, Pedigree: W003020, EXP: 6/12/2014; MELATONIN, Tablet, 3 mg, ND

Code information

CAFFEINE Tablet, 200 mg has the following codes Pedigree: AD21846_37, EXP: 5/1/2014; Pedigree: AD60240_42, EXP: 5/22/2014; Pedigree: W003024, EXP: 6/12/2014; Pedigree: W003725, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 79 of 273

PHYTONADIONE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 25010040515

D-541-2014

Recall number: D-541-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 500 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PHYTONADIONE Tablet, 5 mg may be potentially mislabeled as medroxyPROGESTERone ACETATE, Tablet, 10 mg, NDC 59762374202, Pedigree: AD46312_19, EXP: 5/16/2014; HYDROCORTISONE, Tablet, 5 mg, NDC 00603389919, Pedigree: W003060, EXP: 6/12/2014; GALANTAMINE HBR ER, Capsule, 24 mg, NDC 47335083783, Pedigree: W003735, EXP: 5/31/2014; TORSEMIDE, Tablet, 10 mg, NDC 31722053001,

Code information

PHYTONADIONE Tablet, 5 mg has the following codes Pedigree: AD46312_22, EXP: 4/30/2014; Pedigree: W003061, EXP: 5/31/2014; Pedigree: W003737, EXP: 5/31/2014; Pedigree: AD25452_1, EXP: 4/30/2014; Pedigree: W003440, EXP: 5/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 80 of 273

BISOPROLOL FUMARATE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 29300012601

D-542-2014

Recall number: D-542-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 299 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; BISOPROLOL FUMARATE Tablet, 5 mg may be potentially mislabeled as: ESTROPIPATE, Tablet, 0.75 mg, NDC 00591041401, Pedigree: AD34934_4, EXP: 5/10/2014.

Code information

BISOPROLOL FUMARATE Tablet, 5 mg has the following code Pedigree: AD34934_7, EXP: 5/10/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 81 of 273

CRANBERRY EXTRACT/VITAMIN C Capsule, 450 mg/125 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 31604014271

D-543-2014

Recall number: D-543-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 546 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CRANBERRY EXTRACT/VITAMIN C Capsule, 450 mg/125 mg may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 00536406001, Pedigree: W002653, EXP: 6/5/2014; MODAFINIL, Tablet, 200 mg, NDC 00603466216, Pedigree: W003779, EXP: 6/26/2014; NIACIN ER, Tablet, 500 mg, NDC 00074307490, Pedigree: W003739, EXP: 6/26/2014; GLUCOSAMINE/CHONDROITIN, Capsule, 500 mg/40

Code information

CRANBERRY EXTRACT/VITAMIN C Capsule, 450 mg/125 mg has the following codes Pedigree: W002692, EXP: 6/5/2014; Pedigree: W003715, EXP: 6/26/2014; Pedigree: W003716, EXP: 6/26/2014; Pedigree: AD60240_11, EXP: 5/22/2014; Pedigree: W002693, EXP: 6/5/2014; Pedigree: AD46257_13, EXP: 5/15/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 82 of 273

QUINAPRIL Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 31722027090

D-544-2014

Recall number: D-544-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; QUINAPRIL Tablet, 40 mg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 10 mg, NDC 16714002104, Pedigree: AD52778_73, EXP: 5/21/2014.

Code information

QUINAPRIL Tablet, 40 mg has the following code Pedigree: AD52778_76, EXP: 5/21/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 83 of 273

TORSEMIDE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 31722053001

D-545-2014

Recall number: D-545-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; TORSEMIDE Tablet, 10 mg may be potentially mislabeled as MEXILETINE HCL, Capsule, 200 mg, NDC 00093874001, Pedigree: AD25264_7, EXP: 5/3/2014.

Code information

TORSEMIDE Tablet, 10 mg has the following code Pedigree: AD25264_13, EXP: 5/3/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 84 of 273

MAGNESIUM GLUCONATE Tablet, 500 mg (27 mg Elem Mg), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 35046000322

D-546-2014

Recall number: D-546-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MAGNESIUM GLUCONATE Tablet, 500 mg (27 mg Elem Mg) may be potentially mislabeled as FLUVASTATIN, Capsule, 20 mg, NDC 00378802077, Pedigree: W002655, EXP: 6/4/2014.

Code information

MAGNESIUM GLUCONATE Tablet, 500 mg (27 mg Elem Mg) has the following code Pedigree: W002687, EXP: 6/5/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 85 of 273

MELATONIN Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 35046000391

D-547-2014

Recall number: D-547-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MELATONIN Tablet, 1 mg may be potentially mislabeled as CRANBERRY EXTRACT/VITAMIN C, Capsule, 450 mg/125 mg, NDC 31604014271, Pedigree: W002692, EXP: 6/5/2014; GLYCOPYRROLATE, Tablet, 2 mg, NDC 00603318121, Pedigree: W003252, EXP: 6/17/2014.

Code information

MELATONIN Tablet, 1 mg has the following codes Pedigree: W002695, EXP: 6/5/2014; Pedigree: W003317, EXP: 6/18/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 86 of 273

MULTIVITAMIN/MULTIMINERAL Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 37205018581

D-548-2014

Recall number: D-548-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,045 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MULTIVITAMIN/MULTIMINERAL, Tablet may be potentially mislabeled as QUEtiapine FUMARATE, Tablet, 25 mg, NDC 60505313001, Pedigree: AD33897_25, EXP: 5/9/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: W002512, EXP: 6/3/2014.

Code information

MULTIVITAMIN/MULTIMINERAL Tablet has the following codes Pedigree: AD32328_8, EXP: 5/9/2014; Pedigree: W002513, EXP: 6/3/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 87 of 273

COENZYME Q-10, Capsule 100 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 37205055065

D-549-2014

Recall number: D-549-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 341 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; COENZYME Q-10 Capsule, 100 mg may be potentially mislabeled as ASPIRIN EC, Tablet, 325 mg, NDC 00904201360, Pedigree: AD30180_13, EXP: 5/9/2014; ASPIRIN, Chew Tablet, 81 mg, NDC 00536329736, Pedigree: AD33897_1, EXP: 5/9/2014; TACROLIMUS, Capsule, 1 mg, NDC 00781210301, Pedigree: AD37056_1, EXP: 5/10/2014; METOPROLOL TARTRATE, Tablet, 12.5 mg (1/2 of 25 mg), NDC 576640

Code information

COENZYME Q-10, Capsule, 100 mg has the following codes Pedigree: AD30180_16, EXP: 5/9/2014; Pedigree: AD32325_4, EXP: 5/9/2014; Pedigree: AD37056_4, EXP: 5/10/2014; Pedigree: AD70655_11, EXP: 5/28/2014; Pedigree: W002711, EXP: 6/6/2014; Pedigree: W003871, EXP: 6/27/2014; Pedigree: W003998, EXP: 7/1/2014; Pedigree: AD68019_4, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 88 of 273

NICOTINE POLACRILEX Lozenge, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 37205098769

D-550-2014

Recall number: D-550-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,582 Lozenges

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NICOTINE POLACRILEX Lozenge, 2 mg may be potentially mislabeled as ASPIRIN DR EC, Tablet, 81 mg, NDC 00182106105, Pedigree: AD52433_1, EXP: 5/17/2014; chlorproMAZINE HCl, Tablet, 100 mg, NDC 00832030300, Pedigree: AD70700_1, EXP: 5/29/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD73623_1, EXP: 5/30/2014; FOLIC ACID, Tablet, 1 mg, NDC 65162036110,

Code information

NICOTINE POLACRILEX Lozenge, 2 mg has the following codes Pedigree: AD52433_4, EXP: 5/17/2014; Pedigree: AD70700_4, EXP: 5/29/2014; Pedigree: AD73623_7, EXP: 5/30/2014; Pedigree: W003823, EXP: 6/27/2014; Pedigree: W003463, EXP: 6/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 89 of 273

VITAMIN B COMPLEX PROLONGED RELEASE Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 40985022251

D-551-2014

Recall number: D-551-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 120 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; VITAMIN B COMPLEX PROLONGED RELEASE Tablet may be potentially mislabeled as guaiFENesin ER, Tablet, 600 mg, NDC 63824000815, Pedigree: AD73627_23, EXP: 5/30/2014; TOLTERODINE TARTRATE ER, Capsule, 4 mg, NDC 00009519101, Pedigree: AD73686_1, EXP: 5/31/2014.

Code information

VITAMIN B COMPLEX PROLONGED RELEASE Tablet has the following codes Pedigree: AD73627_26, EXP: 5/30/2014; Pedigree: AD76686_1, EXP: 5/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 90 of 273

VITAMIN B COMPLEX PROLONGED RELEASE Tablet, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 40985022251

D-552-2014

Recall number: D-552-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 182 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; VITAMIN B COMPLEX PROLONGED RELEASE, Tablet, 50 mg may be potentially mislabeled as COENZYME Q-10, Capsule, 100 mg, NDC 37205055065, Pedigree: AD30180_16, EXP: 5/9/2014; DOCUSATE SODIUM, Capsule, 50 mg, NDC 67618010060, Pedigree: AD60211_8, EXP: 5/21/2014; ASPIRIN EC, Tablet, 325 mg, NDC 00904201360, Pedigree: AD39588_1, EXP: 5/13/2014.

Code information

VITAMIN B COMPLEX PROLONGED RELEASE Tablet, 50 mg has the following codes Pedigree: AD30180_19, EXP: 5/9/2014; Pedigree: AD60211_20, EXP: 5/21/2014; Pedigree: AD39588_10, EXP: 5/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 91 of 273

OMEGA-3 FATTY ACID Capsule, 1000 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 40985022921

D-553-2014

Recall number: D-553-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 36,840 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; OMEGA-3 FATTY ACID Capsule, 1000 mg may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 00904052060, Pedigree: AD22865_19, EXP: 5/2/2014; CHOLECALCIFEROL, Capsule, 2000 units, NDC 00536379001, Pedigree: AD30028_7, EXP: 5/8/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: W003054, EXP: 6/12/2014; CHOLECALCIFEROL, Capsule, 2000 units, ND

Code information

OMEGA-3 FATTY ACID Capsule, 1000 mg has the following codes Pedigree: AD21846_1, EXP: 5/1/2014; Pedigree: AD30028_4, EXP: 5/8/2014; Pedigree: W003015, EXP: 6/12/2014; Pedigree: W003710, EXP: 6/26/2014; Pedigree: W003711, EXP: 6/26/2014; Pedigree: AD46257_1, EXP: 5/15/2014; Pedigree: W002965, EXP: 6/10/2014; Pedigree: W003312, EXP: 6/18/2014; Pedigree: AD30028_1, EXP: 5/8/2014; Pedigree: AD46257_4, EXP: 5/15/2014; Pedigree: AD32742_1, EXP: 5/1/2014; Pedigree: AD60240_1, EXP: 5/22/2014; Pedigree: ADWA00002135, EXP: 5/31/2014; Pedigree: W002690, EXP: 6/5/2014; Pedigree: W003313, EXP: 6/18/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 92 of 273

FEXOFENADINE HCL, Tablet 180 mg, Rx only, Distributed by: AidaPak Service, LLC,NDC 41167412003

D-554-2014

Recall number: D-554-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FEXOFENADINE HCL Tablet, 180 mg may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 00536406001, Pedigree: AD62992_8, EXP: 5/23/2014.

Code information

FEXOFENADINE HCL, Tablet, 180 mg has the following code Pedigree: AD62834_1, EXP: 5/23/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 93 of 273

LEVOTHYROXINE/ LIOTHYRONINE Tablet, 19 mcg/4.5 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 42192032901

D-555-2014

Recall number: D-555-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 102 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LEVOTHYROXINE/ LIOTHYRONINE Tablet, 19 mcg/4.5 mcg may be potentially mislabeled as MAGNESIUM GLUCONATE DIHYDRATE, Tablet, 500 mg (27 mg Elemental Magnesium), NDC 60258017201, Pedigree: AD30197_16, EXP: 5/9/2014.

Code information

LEVOTHYROXINE/ LIOTHYRONINE Tablet, 19 mcg/4.5 mcg has the following code Pedigree: AD30197_19, EXP: 3/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 94 of 273

LIOTHYRONINE SODIUM, Tablet, 5 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 42794001802

D-556-2014

Recall number: D-556-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LIOTHYRONINE SODIUM Tablet, 5 mcg may be potentially mislabeled as HYDROCHLOROTHIAZIDE, Tablet, 12.5 mg, NDC 16729018201, Pedigree: AD46414_25, EXP: 5/16/2014.

Code information

LIOTHYRONINE SODIUM Tablet, 5 mcg has the following code Pedigree: AD46414_38, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 95 of 273

LIOTHYRONINE SODIUM, Tablet 25 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 42794001902

D-557-2014

Recall number: D-557-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LIOTHYRONINE SODIUM Tablet, 25 mcg may be potentially mislabeled as guanFACINE HCl, Tablet, 1 mg, NDC 00378116001, Pedigree: AD46414_22, EXP: 5/16/2014; BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, NDC 00574010603, Pedigree: AD68010_4, EXP: 5/28/2014.

Code information

LIOTHYRONINE SODIUM Tablet, 25 mcg has the following codes Pedigree: AD46414_35, EXP: 5/16/2014; Pedigree: AD68010_11, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 96 of 273

PANCRELIPASE DR Capsule, Rx only, Distributed by: AidaPak Service, LLC, NDC 42865010302

D-558-2014

Recall number: D-558-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PANCRELIPASE DR Capsule may be potentially mislabeled as MELATONIN, Tablet, 1 mg, NDC 35046000391, Pedigree: W003317, EXP: 6/18/2014; VERAPAMIL HCL, Tablet, 40 mg, NDC 00591040401, Pedigree: W003170, EXP: 6/13/2014.

Code information

PANCRELIPASE DR, Capsule has the following codes Pedigree: W003354, EXP: 6/19/2014; Pedigree: W003171, EXP: 6/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 97 of 273

HYOSCYAMINE SULFATE ER, Tablet, 0.375 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43199001401

D-559-2014

Recall number: D-559-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 99 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; HYOSCYAMINE SULFATE ER Tablet, 0.375 mg may be potentially mislabeled as SERTRALINE HCL, Tablet, 50 mg, NDC 16714061204, Pedigree: W003575, EXP: 6/24/2014.

Code information

HYOSCYAMINE SULFATE ER Tablet, 0.375 mg has the following code Pedigree: W003576, EXP: 6/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 98 of 273

LACTOBACILLUS ACIDOPHILUS Capsule, 500 Million CFU, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 43292050022

D-560-2014

Recall number: D-560-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 700 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LACTOBACILLUS ACIDOPHILUS, Capsule, 500 Million CFU may be potentially mislabeled as MELATONIN, Tablet, 3 mg, NDC 08770140813, Pedigree: AD46257_56, EXP: 5/15/2014; MELATONIN, Tablet, 3 mg, NDC 08770140813, Pedigree: AD30028_28, EXP: 5/7/2014; CRANBERRY EXTRACT/VITAMIN C, Capsule, 450 mg/125 mg, NDC 31604014271, Pedigree: AD60240_11, EXP: 5/22/2014.

Code information

LACTOBACILLUS ACIDOPHILUS Capsule, 500 Million CFU has the following codes Pedigree: AD46257_28, EXP: 5/15/2014; Pedigree: AD30028_10, EXP: 5/7/2014; Pedigree: AD60240_20, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 99 of 273

VITAMIN B COMPLEX, Tablet Over The Counter, Distributed by: AidaPak Service, LLC, NDC 43292055540

D-561-2014

Recall number: D-561-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; VITAMIN B COMPLEX Tablet may be potentially mislabeled as OMEPRAZOLE/SODIUM BICARBONATE, Capsule, 20 mg/1,100 mg, NDC 11523726503, Pedigree: W003789, EXP: 6/27/2014; prednisoLONE, Tablet, 5 mg, NDC 16477050501, Pedigree: W003627, EXP: 6/25/2014.

Code information

VITAMIN B COMPLEX, Tablet has the following codes Pedigree: W003820, EXP: 6/27/2014; Pedigree: W003628, EXP: 6/25/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 100 of 273

LACTOBACILLUS ACIDOPHILUS Capsule, 500 Million CFU, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 43292055746

D-562-2014

Recall number: D-562-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 999 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LACTOBACILLUS ACIDOPHILUS, Capsule, 500 Million CFU may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: W002694, EXP: 6/5/2014

Code information

LACTOBACILLUS ACIDOPHILUS, Capsule, 500 Million CFU has the following code Pedigree: W002698, EXP: 6/5/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 101 of 273

METHYLERGONOVINE MALEATE Tablet, 0.2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43386014028

D-563-2014

Recall number: D-563-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 112 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; METHYLERGONOVINE MALEATE Tablet, 0.2 mg may be potentially mislabeled as ISOSORBIDE MONONITRATE, Tablet, 20 mg, NDC 62175010701, Pedigree: AD52778_31, EXP: 5/20/2014; LEVOTHYROXINE SODIUM, Tablet, 88 mcg, NDC 00378180701, Pedigree: W003476, EXP: 6/20/2014.

Code information

METHYLERGONOVINE MALEATE, Tablet, 0.2 mg has the following codes Pedigree: AD52778_40, EXP: 5/20/2014; Pedigree: W003477, EXP: 6/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 102 of 273

MISOPROSTOL Tablet, 100 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43386016012

D-564-2014

Recall number: D-564-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 120 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MISOPROSTOL Tablet, 100 mcg may be potentially mislabeled as QUINAPRIL HCL, Tablet, 10 mg, NDC 59762502001, Pedigree: AD42611_4, EXP: 5/14/2014.

Code information

MISOPROSTOL, Tablet, 100 mcg has the following code Pedigree: AD42611_7, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 103 of 273

NIFEDIPINE Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43386044024

D-565-2014

Recall number: D-565-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 202 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NIFEDIPINE Capsule, 10 mg may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL W/FLUORIDE, Chew Tablet, 1 mg (F), NDC 64376081501, Pedigree: AD22609_7, EXP: 5/2/2014; NIFEDIPINE, Capsule, 10 mg, NDC 43386044024, Pedigree: AD23082_7, EXP: 9/23/2013.

Code information

NIFEDIPINE, Capsule, 10 mg has the following codes Pedigree: AD23082_7, EXP: 9/23/2013; Pedigree: AD23082_10, EXP: 9/23/2013.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 104 of 273

ORPHENADRINE CITRATE ER Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 43386048024

D-566-2014

Recall number: D-566-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ORPHENADRINE CITRATE ER Tablet, 100 mg may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 40985022921, Pedigree: W002965, EXP: 6/10/2014.

Code information

ORPHENADRINE CITRATE ER, Tablet, 100 mg has the folowing code Pedigree: W002962, EXP: 6/11/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 105 of 273

ISOMETHEPTENE MUCATE/ DICHLORALPHENAZONE/APAP Capsule, 65 mg/100 mg/325 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 44183044001

D-567-2014

Recall number: D-567-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ISOMETHEPTENE MUCATE/ DICHLORALPHENAZONE/APAP Capsule, 65 mg/100 mg/325 mg may be potentially mislabeled as ALBUTEROL SULFATE ER, Tablet, 4 mg, NDC 00378412201, Pedigree: W003578, EXP: 6/24/2014; LOSARTAN POTASSIUM, Tablet, 25 mg, NDC 16714058102, Pedigree: AD22616_7, EXP: 5/2/2014.

Code information

ISOMETHEPTENE MUCATE/ DICHLORALPHENAZONE/APAP, Capsule, 65 mg/100 mg/325 mg has the following codes Pedigree: W003596, EXP: 5/31/2014; Pedigree: AD22858_1, EXP: 3/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 106 of 273

FEXOFENADINE HCl Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 45802042578

D-568-2014

Recall number: D-568-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FEXOFENADINE HCL Tablet, 60 mg may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 51645090901, Pedigree: W003019, EXP: 6/12/2014; NIACIN TR, Capsule, 500 mg, NDC 00904063160, Pedigree: AD60240_17, EXP: 5/22/2014; CRANBERRY EXTRACT/VITAMIN C, Capsule, 450 mg/125 mg, NDC 31604014271, Pedigree: AD46257_13, EXP: 5/15/2014.

Code information

FEXOFENADINE HCL Tablet, 60 mg has the following codes Pedigree: W003020, EXP: 6/12/2014; Pedigree: AD60240_30, EXP: 5/22/2014; Pedigree: AD46257_50, EXP: 5/15/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 107 of 273

guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 45802049878

D-569-2014

Recall number: D-569-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 500 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; guaiFENesin ER, Tablet, 600 mg may be potentially mislabeled as FENOFIBRATE, Tablet, 54 mg, NDC 00378710077, Pedigree: AD21790_52, EXP: 5/1/2014; FENOFIBRATE, Tablet, 54 mg, NDC 00378710077, Pedigree: W002733, EXP: 6/6/2014; glyBURIDE, Tablet, 2.5 mg, NDC 00093834301, Pedigree: W003688, EXP: 5/31/2014; glyBURIDE, Tablet, 2.5 mg, NDC 00093834301, Pedigree: AD30140_34, E

Code information

guaiFENesin ER, Tablet, 600 mg has the following codes Pedigree: AD21790_58, EXP: 5/1/2014; Pedigree: W002734, EXP: 6/6/2014; Pedigree: W003689, EXP: 6/26/2014; Pedigree: AD30140_37, EXP: 5/7/2014; Pedigree: W003006, EXP: 6/11/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 108 of 273

LORATADINE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 45802065078

D-570-2014

Recall number: D-570-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 799 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LORATADINE Tablet, 10 mg may be potentially mislabeled as GLYCOPYRROLATE, Tablet, 2 mg, NDC 00603318121, Pedigree: W002650, EXP: 6/5/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 05445800022, Pedigree: AD21858_4, EXP: 5/1/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: W003217, EXP: 6/14/2014.

Code information

LORATADINE, Tablet, 10 mg has the following codes Pedigree: W002652, EXP: 6/5/2014; Pedigree: AD22865_7, EXP: 5/2/2014; Pedigree: W003253, EXP: 6/17/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 109 of 273

DESIPRAMINE HCL Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 45963034302

D-571-2014

Recall number: D-571-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 98 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; DESIPRAMINE HCL Tablet, 50 mg may be potentially mislabeled as clomiPRAMINE HCl, Capsule, 50 mg, NDC 51672401205, Pedigree: AD30140_4, EXP: 5/7/2014.

Code information

DESIPRAMINE HCL, Tablet, 50 mg has the following code Pedigree: AD30140_7, EXP: 5/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 110 of 273

ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/250 mg/65 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 46122010478

D-572-2014

Recall number: D-572-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/250 mg/65 mg may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Chew Tablet, NDC 00536344308, Pedigree: W003714, EXP: 6/26/2014.

Code information

ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/250 mg/65 mg has the following code Pedigree: W003722, EXP: 4/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 111 of 273

buPROPion HCl ER Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 47335073886

D-573-2014

Recall number: D-573-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; buPROPion HCl ER Tablet, 200 mg may be potentially mislabeled as AMANTADINE HCL, Capsule, 100 mg, NDC 00781204801, Pedigree: W002726, EXP: 6/6/2014.

Code information

buPROPion HCl ER, Tablet, 200 mg has the following code Pedigree: W002727, EXP: 6/6/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 112 of 273

GALANTAMINE HBR ER Capsule, 24 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 47335083783

D-574-2014

Recall number: D-574-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; GALANTAMINE HBR ER, Capsule, 24 mg may be potentially mislabeled as ESCITALOPRAM, Tablet, 5 mg, NDC 00093585001, Pedigree: W003733, EXP: 6/26/2014.

Code information

GALANTAMINE HBR ER, Capsule, 24 mg has the following code Pedigree: W003735, EXP: 5/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 113 of 273

QUETIAPINE FUMARATE Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 47335090288

D-575-2014

Recall number: D-575-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; QUETIAPINE FUMARATE Tablet, 12.5 mg (1/2 of 25 mg) may be potentially mislabeled as SIMVASTATIN, Tablet, 40 mg, NDC 00093715598, Pedigree: AD22845_4, EXP: 5/2/2014.

Code information

QUETIAPINE FUMARATE, Tablet, 12.5 mg (1/2 of 25 mg) has the following code Pedigree: AD21790_79, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 114 of 273

MELATONIN Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 47469000466

D-576-2014

Recall number: D-576-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 360 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MELATONIN, Tablet, 1 mg may be potentially mislabeled as hydrOXYzine PAMOATE, Capsule, 100 mg, NDC 00555032402, Pedigree: AD46265_28, EXP: 5/15/2014; GLUCOSAMINE/CHONDROITIN DS, Tablet, 500 mg/400 mg, NDC 00904559293, Pedigree: AD60211_17, EXP: 5/22/2014.

Code information

MELATONIN, Tablet, 1 mg has the following codes Pedigree: AD46257_19, EXP: 5/15/2014; Pedigree: AD60240_14, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 115 of 273

NITROFURANTOIN MONOHYDRATE/ MACROCRYSTALS Capsule, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 47781030301

D-577-2014

Recall number: D-577-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NITROFURANTOIN MONOHYDRATE/ MACROCRYSTALS, Capsule, 100 mg may be potentially mislabeled as MINOCYCLINE HCL, Capsule, 50 mg, NDC 00591569401, Pedigree: AD52778_46, EXP: 5/20/2014.

Code information

NITROFURANTOIN MONOHYDRATE/ MACROCRYSTALS, Capsule, 100 mg has the following code Pedigree: AD52778_58, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 116 of 273

NITROFURANTOIN MACROCRYSTALS Capsule, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 47781030701

D-578-2014

Recall number: D-578-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 102 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NITROFURANTOIN MACROCRYSTALS Capsule, 50 mg may be potentially mislabeled as PHYTONADIONE, Tablet, 5 mg, NDC 25010040515, Pedigree: AD25452_1, EXP: 4/30/2014.

Code information

NITROFURANTOIN MACROCRYSTALS, Capsule, 50 mg has the following code Pedigree: AD25452_4, EXP: 5/3/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 117 of 273

LACTOBACILLUS GG Capsule, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49100036374

D-579-2014

Recall number: D-579-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,970 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LACTOBACILLUS GG Capsule may be potentially mislabeled as VITAMIN B COMPLEX W/C, Capsule, NDC 54629008001, Pedigree: AD39560_4, EXP: 5/13/2014; DOCUSATE SODIUM, Capsule, 50 mg, NDC 67618010060, Pedigree: AD65457_13, EXP: 5/24/2014; VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet, NDC 60258016001, Pedigree: AD70655_17, EXP: 5/28/2014; TACROLIMUS, Capsule, 1 mg, NDC 00781210

Code information

LACTOBACILLUS GG, Capsule has the following codes Pedigree: AD39588_4, EXP: 5/13/2014 Pedigree: AD65457_16, EXP: 5/24/2014 Pedigree: AD70655_8, EXP: 5/29/2014 Pedigree: AD73627_17, EXP: 5/30/2014 Pedigree: W003051, EXP: 6/12/2014 Pedigree: W003216, EXP: 6/14/2014 Pedigree: AD42584_12, EXP: 5/14/2014 Pedigree: AD46300_11, EXP: 5/15/2014 Pedigree: W002968, EXP: 6/11/2014 Pedigree: AD68019_1, EXP: 5/28/2014 Pedigree: W003172, EXP: 6/13/2014 Pedigree: W003173, EXP: 6/13/2014

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 118 of 273

LACTOBACILLUS GG Capsule, 10 Billion Cells, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49100036374

D-580-2014

Recall number: D-580-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Cells

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LACTOBACILLUS GG Capsule, 10 Billion Cells may be potentially mislabeled as guaiFENesin ER, Tablet, 600 mg, NDC 63824000815, Pedigree: AD21965_22, EXP: 5/1/2014.

Code information

LACTOBACILLUS GG, Capsule, 10 Billion Cells has the following code Pedigree: AD21965_19, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 119 of 273

LACTOBACILLUS GG Capsule, 15 Billion Cells, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49100036374

D-581-2014

Recall number: D-581-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 630 Cells

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LACTOBACILLUS GG Capsule, 15 Billion Cells may be potentially mislabeled as ASPIRIN EC, Tablet, 325 mg, NDC 00904201360, Pedigree: W003356, EXP: 6/19/2014; ZONISAMIDE, Capsule, 100 mg, NDC 64679099001, Pedigree: W003786, EXP: 6/27/2014; VENLAFAXINE HCL, Tablet, 25 mg, NDC 00093019901, Pedigree: W003860, EXP: 6/27/2014.

Code information

LACTOBACILLUS GG, Capsule, 15 Billion Cells has the following codes Pedigree: W003357, EXP: 6/19/2014; Pedigree: W003787, EXP: 6/27/2014; Pedigree: W003869, EXP: 6/27/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 120 of 273

ASPIRIN Tablet, 325 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49348000123

D-582-2014

Recall number: D-582-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ASPIRIN Tablet, 325 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: W002642, EXP: 6/4/2014.

Code information

ASPIRIN, Tablet, 325 mg has the following code Pedigree: W002640, EXP: 6/4/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 121 of 273

D-ALPHA TOCOPHERYL ACETATE Capsule, 400 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49348041010

D-583-2014

Recall number: D-583-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 107 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; D-ALPHA TOCOPHERYL ACETATE Capsule, 400 units may be potentially mislabeled as CYANOCOBALAMIN, Tablet, 500 mcg, NDC 00536355101, Pedigree: AD52993_19, EXP: 5/20/2014.

Code information

D-ALPHA TOCOPHERYL ACETATE, Capsule, 400 units has the following code Pedigree: AD52993_28, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 122 of 273

NICOTINE POLACRILEX Lozenge, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 49348085216

D-584-2014

Recall number: D-584-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 70 Lozenges

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NICOTINE POLACRILEX Lozenge, 2 mg may be potentially mislabeled as VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet, NDC 60258016001, Pedigree: W003361, EXP: 6/19/2014.

Code information

NICOTINE POLACRILEX, Lozenge, 2 mg has the following code Pedigree: W003393, EXP: 6/19/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 123 of 273

ASPIRIN EC DR Tablet, 81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 49348098015

D-585-2014

Recall number: D-585-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 544 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ASPIRIN EC DR Tablet, 81 mg may be potentially mislabeled as MELATONIN, Tablet, 3 mg, NDC 51991001406, Pedigree: AD28322_7, EXP: 5/6/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00904789159, Pedigree: W003671, EXP: 6/25/2014.

Code information

ASPIRIN EC DR, Tablet, 81 mg has the following codes Pedigree: AD28349_1, EXP: 2/28/2014; Pedigree: W003672, EXP: 2/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 124 of 273

GLYCOPYRROLATE Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 49884006601

D-586-2014

Recall number: D-586-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; GLYCOPYRROLATE Tablet, 2 mg may be potentially mislabeled as LACTOBACILLUS, Tablet, NDC 64980012950, Pedigree: W003624, EXP: 1/31/2014.

Code information

GLYCOPYRROLATE, Tablet, 2 mg has the following code Pedigree: W003625, EXP: 6/25/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 125 of 273

DOXEPIN HCL Capsule, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 49884022201

D-587-2014

Recall number: D-587-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; DOXEPIN HCL Capsule, 150 mg may be potentially mislabeled as VALSARTAN, Tablet, 160 mg, NDC 00078035934, Pedigree: AD46312_7, EXP: 5/16/2014.

Code information

DOXEPIN HCL, Capsule, 150 mg has the following code Pedigree: AD46312_10, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 126 of 273

DOXYCYCLINE MONOHYDRATE Capsule, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 49884072703

D-588-2014

Recall number: D-588-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 799 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; DOXYCYCLINE MONOHYDRATE Capsule, 100 mg may be potentially mislabeled as diphenhydrAMINE HCl, Tablet, 25 mg, NDC 00904555159, Pedigree: AD67992_4, EXP: 5/28/2014; DUTASTERIDE, Capsule, 0.5 mg, NDC 00173071215, Pedigree: AD52778_4, EXP: 5/20/2014.

Code information

DOXYCYCLINE MONOHYDRATE, Capsule, 100 mg has the following codes Pedigree: AD65323_7, EXP: 5/28/2014; Pedigree: AD52778_25, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 127 of 273

DILTIAZEM HCL ER Capsule, 240 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 49884083109

D-589-2014

Recall number: D-589-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; DILTIAZEM HCL ER Capsule, 240 mg may be potentially mislabeled as NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 37205098769, Pedigree: AD52433_4, EXP: 5/17/2014; PARoxetine HCl, Tablet, 10 mg, NDC 13107015430, Pedigree: AD52778_67, EXP: 5/20/2014.

Code information

DILTIAZEM HCL ER, Capsule, 240 mg has the following codes Pedigree: AD52375_1, EXP: 5/17/2014; Pedigree: AD56917_1, EXP: 5/21/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 128 of 273

HYDRALAZINE HCL Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111032701

D-590-2014

Recall number: D-590-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; HYDRALAZINE HCL Tablet, 25 mg may be potentially mislabeled as DOCUSATE CALCIUM, Capsule, 240 mg, NDC 00536375501, Pedigree: AD49582_16, EXP: 5/16/2014.

Code information

HYDRALAZINE HCL, Tablet, 25 mg has the following code Pedigree: AD49610_4, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 129 of 273

hydrALAZINE HCl Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111032801

D-591-2014

Recall number: D-591-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; hydrALAZINE HCl Tablet, 50 mg may be potentially mislabeled as CapsuleTOPRIL, Tablet, 12.5 mg, NDC 00143117101, Pedigree: AD52778_16, EXP: 5/20/2014.

Code information

hydrALAZINE HCl, Tablet, 50 mg has the following code Pedigree: AD52778_28, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 130 of 273

traZODone HCl Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111043301

D-592-2014

Recall number: D-592-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 400 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; traZODone HCl Tablet, 50 mg may be potentially mislabeled as DEXAMETHASONE, Tablet, 1 mg, NDC 00054418125, Pedigree: AD37088_1, EXP: 5/9/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD54498_4, EXP: 5/20/2014; guanFACINE HCl, Tablet, 1 mg, NDC 00591044401, Pedigree: AD39611_1, EXP: 4/30/2014.

Code information

traZODone HCl, Tablet, 50 mg has the following codes Pedigree: AD37088_4, EXP: 5/9/2014; Pedigree: AD54562_1, EXP: 5/20/2014; Pedigree: AD39611_4, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 131 of 273

traZODone HCl Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111043303

D-593-2014

Recall number: D-593-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,000 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; traZODone HCl Tablet, 50 mg may be potentially mislabeled as AMANTADINE HCL, Tablet, 100 mg, NDC 00832011100, Pedigree: AD54475_1, EXP: 5/20/2014.

Code information

traZODone HCl, Tablet, 50 mg has the following code Pedigree: AD54475_7, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 132 of 273

traZODone HCl Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111044101

D-594-2014

Recall number: D-594-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; traZODone HCl Tablet, 150 mg may be potentially mislabeled as NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 00135051001, Pedigree: AD21858_1, EXP: 5/1/2014; SENNOSIDES, Tablet, 8.6 mg, NDC 00182109301, Pedigree: W003256, EXP: 6/17/2014.

Code information

traZODone HCl, Tablet, 150 mg has the following codes Pedigree: AD21858_7, EXP: 5/1/2014; Pedigree: W003245, EXP: 6/17/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 133 of 273

TORSEMIDE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50111091601

D-595-2014

Recall number: D-595-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; TORSEMIDE, Tablet, 10 mg may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 00536440801, Pedigree: AD30197_22, EXP: 5/9/2014.

Code information

TORSEMIDE, Tablet, 10 mg has the following code Pedigree: AD30197_25, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 134 of 273

RIVAROXABAN Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50458057930

D-596-2014

Recall number: D-596-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; RIVAROXABAN Tablet, 20 mg may be potentially mislabeled as VENLAFAXINE HCL, Tablet, 100 mg, NDC 00093738301, Pedigree: W002619, EXP: 6/4/2014.

Code information

RIVAROXABAN, Tablet, 20 mg has the following code Pedigree: W002620, EXP: 6/4/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 135 of 273

TACROLIMUS Capsule, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 50742020801

D-597-2014

Recall number: D-597-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; TACROLIMUS, Capsule, 1 mg may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 125 mcg, NDC 00074706890, Pedigree: AD70633_4, EXP: 5/23/2014.

Code information

TACROLIMUS, Capsule, 1 mg has the following code Pedigree: AD60590_1, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 136 of 273

SOLIFENACIN SUCCINATE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51248015001

D-598-2014

Recall number: D-598-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; SOLIFENACIN SUCCINATE Tablet, 5 mg may be potentially mislabeled as BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, NDC 00574010601, Pedigree: W003754, EXP: 6/26/2014.

Code information

SOLIFENACIN SUCCINATE, Tablet, 5 mg has the following code Pedigree: W003755, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 137 of 273

PYRIDOXINE HCL Tablet, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 51645090901

D-599-2014

Recall number: D-599-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 600 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PYRIDOXINE HCL Tablet, 50 mg may be potentially mislabeled as CALCIUM CITRATE, Tablet, 950 mg (200 mg Elem Ca), NDC 00904506260, Pedigree: W002699, EXP: 6/5/2014; MULTIVITAMIN/MULTIMINERAL W/IRON, Chew Tablet, NDC 00536781601, Pedigree: W003018, EXP: 6/12/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: W003705, EXP: 6/25/2014; LACTASE ENZYME, Tab

Code information

PYRIDOXINE HCL, Tablet, 50 mg has the following codes Pedigree: W002697, EXP: 6/5/2014; Pedigree: W003019, EXP: 6/12/2014; Pedigree: W003718, EXP: 6/26/2014; Pedigree: AD46257_25, EXP: 5/15/2014; Pedigree: AD73521_25, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 138 of 273

clomiPRAMINE HCl Capsule, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51672401205

D-600-2014

Recall number: D-600-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 450 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; clomiPRAMINE HCl Capsule, 50 mg may be potentially mislabeled as guanFACINE HCl, Tablet, 1 mg, NDC 00378116001, Pedigree: AD46265_25, EXP: 5/15/2014; CHLORTHALIDONE, Tablet, 50 mg, NDC 00378021301, Pedigree: W002988, EXP: 6/11/2014; AMANTADINE HCL, Capsule, 100 mg, NDC 00781204801, Pedigree: W003674, EXP: 6/25/2014; ISOSORBIDE MONONITRATE, Tablet, 10 mg, NDC 6217501060

Code information

clomiPRAMINE HCl, Capsule, 50 mg has the following codes Pedigree: AD46265_1, EXP: 5/15/2014; Pedigree: W002998, EXP: 6/11/2014; Pedigree: W003675, EXP: 6/25/2014; Pedigree: AD30140_4, EXP: 5/7/2014; Pedigree: AD73525_4, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 139 of 273

ETODOLAC Tablet, 400 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51672401801

D-601-2014

Recall number: D-601-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 101 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ETODOLAC, Tablet, 400 mg may be potentially mislabeled as PANCRELIPASE DR, Capsule, 12000 /38000 /60000 USP units, NDC 00032121201, Pedigree: W003731, EXP: 6/26/2014.

Code information

ETODOLAC, Tablet, 400 mg has the following code Pedigree: W003734, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 140 of 273

WARFARIN SODIUM Tablet, 0.5 mg (1/2 of 1 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 51672402701

D-602-2014

Recall number: D-602-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; WARFARIN SODIUM, Tablet, 0.5 mg (1/2 of 1 mg) may be potentially mislabeled as SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: AD70636_1, EXP: 5/29/2014.

Code information

WARFARIN SODIUM, Tablet, 0.5 mg (1/2 of 1 mg) has the following code Pedigree: AD60590_4, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 141 of 273

WARFARIN SODIUM Tablet, 0.5 mg (1/2 of 1 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 51672402701

D-603-2014

Recall number: D-603-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; WARFARIN SODIUM Tablet, 0.5 mg (1/2 of 1 mg) may be potentially mislabeled as SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: AD70636_1, EXP: 5/29/2014.

Code information

WARFARIN SODIUM Tablet, 0.5 mg (1/2 of 1 mg) has the following code Pedigree: AD60590_4, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 142 of 273

carBAMazepine ER Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51672412401

D-604-2014

Recall number: D-604-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; carBAMazepine ER Tablet, 200 mg may be potentially mislabeled as ACARBOSE, Tablet, 25 mg, NDC 00054014025, Pedigree: AD60272_1, EXP: 5/22/2014.

Code information

carBAMazepine ER, Tablet, 200 mg has the following code Pedigree: AD60272_7, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 143 of 273

MELATONIN Tablet, 3 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 51991001406

D-605-2014

Recall number: D-605-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 718 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MELATONIN Tablet, 3 mg may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD25452_13, EXP: 5/3/2014; PIOGLITAZONE, Tablet, 15 mg, NDC 00591320530, Pedigree: AD28322_4, EXP: 4/30/2014; COENZYME Q-10, Capsule, 100 mg, NDC 37205055065, Pedigree: AD70655_11, EXP: 5/28/2014; COENZYME Q-10, Capsule, 100 mg, NDC 37205055065, Pedigree

Code information

MELATONIN, Tablet, 3 mg has the following codes Pedigree: AD25452_16, EXP: 5/3/2014; Pedigree: AD28322_7, EXP: 5/6/2014; Pedigree: AD70655_14, EXP: 5/28/2014; Pedigree: W003999, EXP: 7/1/2014; Pedigree: AD32325_7, EXP: 5/9/2014; Pedigree: AD68019_7, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 144 of 273

PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 51991056601

D-606-2014

Recall number: D-606-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,399 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet may be potentially mislabeled as COLCHICINE, Tablet, 0.6 mg, NDC 64764011907, Pedigree: AD65457_1, EXP: 5/23/2014; GALANTAMINE HBr ER, Capsule, 8 mg, NDC 10147089103, Pedigree: W003509, EXP: 6/21/2014; BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, NDC 00781532531, Pedigree: AD32579_7, EXP: 5/9/2014; CINACALCET HCL, Tablet, 30 mg, N

Code information

PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet has the following codes Pedigree: AD62829_18, EXP: 5/24/2014; Pedigree: W003511, EXP: 6/21/2014; Pedigree: AD32579_4, EXP: 5/9/2014; Pedigree: AD73597_16, EXP: 5/31/2014; Pedigree: W003086, EXP: 6/12/2014; Pedigree: W003034, EXP: 6/12/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 145 of 273

NEOMYCIN SULFATE Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 51991073801

D-607-2014

Recall number: D-607-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; NEOMYCIN SULFATE, Tablet, 500 mg may be potentially mislabeled as IMIPRAMINE HCL, Tablet, 25 mg, NDC 00781176401, Pedigree: AD49448_10, EXP: 5/17/2014.

Code information

NEOMYCIN SULFATE, Tablet, 500 mg has the following code Pedigree: AD49448_17, EXP: 5/17/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 146 of 273

FIDAXOMICIN Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 52015008001

D-608-2014

Recall number: D-608-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 120 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FIDAXOMICIN Tablet, 200 mg may be potentially mislabeled as BENAZEPRIL HCL, Tablet, 40 mg, NDC 65162075410, Pedigree: W003918, EXP: 6/28/2014.

Code information

FIDAXOMICIN, Tablet, 200 mg has the following code Pedigree: W003920, EXP: 6/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 147 of 273

HYDROcodone BITARTRATE/ ACETAMINOPHEN Tablet, 7.5 mg/325 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 52544016201

D-609-2014

Recall number: D-609-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; HYDROcodone BITARTRATE/ ACETAMINOPHEN, Tablet, 7.5 mg/325 mg may be potentially mislabeled as MELATONIN, Tablet, 3 mg, NDC 51991001406, Pedigree: W003999, EXP: 7/1/2014.

Code information

HYDROcodone BITARTRATE/ ACETAMINOPHEN, Tablet, 7.5 mg/325 mg has the following code Pedigree: W004005, EXP: 7/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 148 of 273

CHOLECALCIFEROL Capsule, 50000 units, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 53191036201

D-610-2014

Recall number: D-610-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CHOLECALCIFEROL Capsule, 50000 units may be potentially mislabeled as FENOFIBRATE, Tablet, 54 mg, NDC 00378710077, Pedigree: AD60272_64, EXP: 5/22/2014.

Code information

CHOLECALCIFEROL, Capsule, 50000 units has the following code Pedigree: AD60268_4, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 149 of 273

DOXYCYCLINE HYCLATE Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 53489012002

D-611-2014

Recall number: D-611-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 50 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; DOXYCYCLINE HYCLATE, Tablet, 100 mg may be potentially mislabeled as DESLORATADINE, Tablet, 5 mg, NDC 00085126401, Pedigree: AD30993_5, EXP: 2/28/2014.

Code information

DOXYCYCLINE HYCLATE Tablet, 100 mg has the following code Pedigree: AD30993_8, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 150 of 273

TRIMETHOBENZAMIDE HCl Capsule, 300 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 53489037601

D-612-2014

Recall number: D-612-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; TRIMETHOBENZAMIDE HCl, Capsule, 300 mg may be potentially mislabeled as GABAPENTIN, Tablet, 600 mg, NDC 00228263611, Pedigree: AD21965_7, EXP: 5/1/2014; CHOLECALCIFEROL, Capsule, 5000 units, NDC 00904598660, Pedigree: AD70629_19, EXP: 5/29/2014; SODIUM BICARBONATE, Tablet, 650 mg, NDC 64980018210, Pedigree: W002970, EXP: 6/11/2014.

Code information

TRIMETHOBENZAMIDE HCl, Capsule, 300 mg has the following codes Pedigree: AD21858_10, EXP: 5/1/2014; Pedigree: AD70625_1, EXP: 5/29/2014; Pedigree: W002976, EXP: 6/11/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 151 of 273

MESALAMINE CR Capsule, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 54092018981

D-613-2014

Recall number: D-613-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 240 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MESALAMINE CR, Capsule, 250 mg may be potentially mislabeled as ASPIRIN EC, Tablet, 325 mg, NDC 00904201360, Pedigree: AD52378_1, EXP: 5/17/2014.

Code information

MESALAMINE CR, Capsule, 250 mg has the following code Pedigree: AD52412_1, EXP: 5/17/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 152 of 273

MESALAMINE CR Capsule, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 54092019112

D-614-2014

Recall number: D-614-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 111 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; MESALAMINE CR, Capsule, 500 mg may be potentially mislabeled as clomiPRAMINE HCl, Capsule, 50 mg, NDC 51672401205, Pedigree: AD21790_7, EXP: 5/1/2014.

Code information

MESALAMINE CR, Capsule, 500 mg has the following code Pedigree: AD21965_16, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 153 of 273

LANTHANUM CARBONATE Chew Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 54092025290

D-615-2014

Recall number: D-615-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 405 Chew Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LANTHANUM CARBONATE Chew Tablet, 500 mg may be potentially mislabeled as ISONIAZID, Tablet, 300 mg, NDC 00555007102, Pedigree: AD32757_31, EXP: 5/13/2014; CYANOCOBALAMIN, Tablet, 1000 mcg, NDC 00536355601, Pedigree: AD32757_53, EXP: 5/14/2014; MAGNESIUM CHLORIDE, Tablet, 64 mg, NDC 68585000575, Pedigree: W002712, EXP: 6/6/2014; MAGNESIUM CHLORIDE, Tablet, 64 mg, NDC 68

Code information

LANTHANUM CARBONATE, Chew Tablet, 500 mg has the following codes Pedigree: AD32764_5, EXP: 5/13/2014; Pedigree: AD32764_8, EXP: 5/14/2014; Pedigree: W002790, EXP: 6/6/2014; Pedigree: W003410, EXP: 6/19/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 154 of 273

GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 54458010022

D-616-2014

Recall number: D-616-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; GLUCOSAMINE/CHONDROITIN Capsule, 500 mg/400 mg may be potentially mislabeled as FEXOFENADINE HCL, Tablet, 60 mg, NDC 45802042578, Pedigree: AD60240_30, EXP: 5/22/2014.

Code information

GLUCOSAMINE/CHONDROITIN, Capsule, 500 mg/400 mg has the following code Pedigree: AD60240_33, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 155 of 273

VITAMIN B COMPLEX W/C Capsule, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 54629008001

D-617-2014

Recall number: D-617-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,398 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; VITAMIN B COMPLEX W/C Capsule may be potentially mislabeled as SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: AD39560_1, EXP: 5/13/2014.

Code information

VITAMIN B COMPLEX W/C, Capsule has the following code Pedigree: AD39560_4, EXP: 5/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 156 of 273

LACTOBACILLUS ACIDOPHILUS Capsule, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 54629011101

D-618-2014

Recall number: D-618-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 2,392 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; LACTOBACILLUS ACIDOPHILUS Capsule may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 2000 units, NDC 00904615760, Pedigree: AD65311_1, EXP: 5/24/2014; PANCRELIPASE DR, Capsule, 24000 /76000 /120000 USP units, NDC 00032122401, Pedigree: AD65457_4, EXP: 5/24/2014.

Code information

LACTOBACILLUS ACIDOPHILUS, Capsule has the following codes Pedigree: AD65311_7, EXP: 5/24/2014; Pedigree: AD65311_4, EXP: 5/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 157 of 273

OLANZapine Tablet, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 55111016530

D-619-2014

Recall number: D-619-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 210 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; OLANZapine, Tablet, 7.5 mg may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 175 mcg, NDC 00527135001, Pedigree: AD46265_37, EXP: 5/15/2014; LEVOTHYROXINE SODIUM, Tablet, 88 mcg, NDC 00781518392, Pedigree: AD60272_73, EXP: 5/22/2014; MIRTAZAPINE, Tablet, 7.5 mg, NDC 59762141503, Pedigree: AD73525_55, EXP: 5/30/2014.

Code information

OLANZapine, Tablet, 7.5 mg has the following codes Pedigree: AD46265_46, EXP: 5/15/2014; Pedigree: AD60272_79, EXP: 5/22/2014; Pedigree: AD73525_58, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 158 of 273

tiZANidine HCl Tablet, 1 mg (1/2 of 2 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 55111017915

D-620-2014

Recall number: D-620-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 299 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; tiZANidine HCl Tablet, 1 mg (1/2 of 2 mg) may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 00536440801, Pedigree: AD60428_10, EXP: 5/22/2014.

Code information

tiZANidine HCl, Tablet, 1 mg (1/2 of 2 mg) has the following code Pedigree: AD60272_52, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 159 of 273

tiZANidine HCl Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 55111017915

D-621-2014

Recall number: D-621-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 600 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; tiZANidine HCl Tablet, 2 mg may be potentially mislabeled as RIBAVIRIN, Capsule, 200 mg, NDC 68382026007, Pedigree: AD21790_37, EXP: 4/30/2014; CYANOCOBALAMIN, Tablet, 1000 mcg, NDC 00904421713, Pedigree: AD46257_59, EXP: 5/15/2014; NIACIN, Tablet, 100 mg, NDC 00904227160, Pedigree: W002661, EXP: 6/5/2014; PANTOPRAZOLE SODIUM DR, Tablet, 20 mg, NDC 00008060601, Pedigree

Code information

tiZANidine HCl, Tablet, 2 mg has the following codes Pedigree: AD21790_40, EXP: 5/1/2014; Pedigree: AD46265_16, EXP: 5/15/2014; Pedigree: W002663, EXP: 6/5/2014; Pedigree: AD73525_31, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 160 of 273

GLIMEPIRIDE Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 55111032001

D-622-2014

Recall number: D-622-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; GLIMEPIRIDE, Tablet, 1 mg may be potentially mislabeled as clomiPRAMINE HCl, Capsule, 50 mg, NDC 51672401205, Pedigree: AD73525_4, EXP: 5/30/2014.

Code information

GLIMEPIRIDE, Tablet, 1 mg has the following code Pedigree: AD73525_10, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 161 of 273

MODAFINIL Tablet, 50 mg (1/2 of 100 mg Tablet), Rx only, Distributed by: AidaPak Service, LLC, NDC 55253080130

D-623-2014

Recall number: D-623-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MODAFINIL Tablet, 50 mg (1/2 of 100 mg Tablet) may be potentially mislabeled as SACCHAROMYCES BOULARDII LYO, Capsule, 250 mg, NDC 00414200007, Pedigree: AD21859_1, EXP: 10/31/2013.

Code information

MODAFINIL Tablet, 50 mg (1/2 of 100 mg Tablet) has the following code Pedigree: AD21787_4, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 162 of 273

CINACALCET HCL Tablet, 30 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 55513007330

D-624-2014

Recall number: D-624-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 600 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; CINACALCET HCL, Tablet, 30 mg may be potentially mislabeled as ACETAMINOPHEN, Chew Tablet, 80 mg, NDC 00536323307, Pedigree: W003113, EXP: 6/13/2014; FERROUS SULFATE, Tablet, 325 mg (65 mg Elemental Iron), NDC 00904759160, Pedigree: AD54553_1, EXP: 5/20/2014; OMEGA-3-ACID ETHYL ESTERS, Capsule, 1000 mg, NDC 00173078302, Pedigree: AD32757_40, EXP: 5/14/2014; COLCHICINE,

Code information

CINACALCET HCL, Tablet, 30 mg has the following codes Pedigree: W003168, EXP: 6/13/2014; Pedigree: AD54516_4, EXP: 5/20/2014; Pedigree: AD32757_50, EXP: 5/14/2014; Pedigree: W003615, EXP: 6/25/2014; Pedigree: AD52778_82, EXP: 5/21/2014; Pedigree: AD73597_13, EXP: 5/31/2014; Pedigree: W003481, EXP: 6/20/2014; Pedigree: W003492, EXP: 6/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 163 of 273

CINACALCET HCL Tablet, 60 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 55513007430

D-625-2014

Recall number: D-625-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; CINACALCET HCL Tablet, 60 mg may be potentially mislabeled as RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: W003741, EXP: 6/26/2014.

Code information

CINACALCET HCL, Tablet, 60 mg has the following code Pedigree: W003742, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 164 of 273

traMADol HCl Tablet, 25 mg (1/2 of 50 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 57664037708

D-626-2014

Recall number: D-626-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; traMADol HCl Tablet, 25 mg (1/2 of 50 mg) may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 137 mcg, NDC 00527163801, Pedigree: AD60272_76, EXP: 5/22/2014.

Code information

traMADol HCl, Tablet, 25 mg (1/2 of 50 mg) has the following code Pedigree: AD60272_92, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 165 of 273

tiZANidine HCL Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050289

D-627-2014

Recall number: D-627-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 299 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; tiZANidine HCL Tablet, 2 mg may be potentially mislabeled as NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 37205098769, Pedigree: AD70700_4, EXP: 5/29/2014; NIFEdipine ER, Tablet, 60 mg, NDC 00591319401, Pedigree: W003729, EXP: 6/26/2014.

Code information

tiZANidine HCL, Tablet, 2 mg has the following codes Pedigree: AD70700_10, EXP: 5/29/2014; Pedigree: W003750, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 166 of 273

METOPROLOL TARTRATE Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050652

D-628-2014

Recall number: D-628-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 402 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; METOPROLOL TARTRATE Tablet, 12.5 mg (1/2 of 25 mg) may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00904789159, Pedigree: AD68022_1, EXP: 5/28/2014; METOPROLOL TARTRATE, Tablet, 12.5 mg (1/2 of 25 mg), NDC 57664050652, Pedigree: AD68010_14, EXP: 5/28/2014.

Code information

METOPROLOL TARTRATE, Tablet, 12.5 mg (1/2 of 25 mg) has the following codes Pedigree: AD68010_14, EXP: 5/28/2014; Pedigree: AD68010_17, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 167 of 273

METOPROLOL TARTRATE Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050652

D-629-2014

Recall number: D-629-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; METOPROLOL TARTRATE, Tablet, 25 mg may be potentially mislabeled as ASCORBIC ACID, Tablet, 250 mg, NDC 00904052260, Pedigree: W003826, EXP: 6/27/2014; amLODIPine BESYLATE, Tablet, 5 mg, NDC 00093716798, Pedigree: W002840, EXP: 6/7/2014.

Code information

METOPROLOL TARTRATE, Tablet, 25 mg has the following codes Pedigree: W003843, EXP: 6/27/2014; Pedigree: W002841, EXP: 6/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 168 of 273

CITALOPRAM Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664050788

D-630-2014

Recall number: D-630-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 299 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; CITALOPRAM Tablet, 10 mg may be potentially mislabeled as OXYBUTYNIN CHLORIDE, Tablet, 5 mg, NDC 00603497521, Pedigree: AD52778_61, EXP: 5/20/2014; COENZYME Q-10, Capsule, 30 mg, NDC 00904501546, Pedigree: W002814, EXP: 6/7/2014.

Code information

CITALOPRAM, Tablet, 10 mg has the following codes Pedigree: AD56921_1, EXP: 5/21/2014; Pedigree: W002844, EXP: 6/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 169 of 273

ISOSORBIDE DINITRATE ER Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57664060088

D-631-2014

Recall number: D-631-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ISOSORBIDE DINITRATE ER Tablet, 40 mg may be potentially mislabeled as CILOSTAZOL, Tablet, 50 mg, NDC 60505252101, Pedigree: AD21811_7, EXP: 5/1/2014.

Code information

ISOSORBIDE DINITRATE ER, Tablet, 40 mg has the following code Pedigree: AD23082_4, EXP: 5/3/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 170 of 273

PIMOZIDE Tablet, 1 mg (1/2 of 2 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 57844018701

D-632-2014

Recall number: D-632-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; PIMOZIDE Tablet, 1 mg (1/2 of 2 mg) may be potentially mislabeled as METOPROLOL TARTRATE, Tablet, 12.5 mg (1/2 of 25 mg), NDC 63304057901, Pedigree: AD73525_52, EXP: 5/30/2014.

Code information

PIMOZIDE, Tablet, 1 mg (1/2 of 2 mg) has the following code Pedigree: AD73525_61, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 171 of 273

PIMOZIDE Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 57844018701

D-633-2014

Recall number: D-633-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; PIMOZIDE Tablet, 2 mg may be potentially mislabeled as DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: AD30140_31, EXP: 5/7/2014.

Code information

PIMOZIDE, Tablet, 2 mg has the following code Pedigree: AD30140_43, EXP: 5/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 172 of 273

DOCUSATE SODIUM Capsule, 100 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 57896040110

D-634-2014

Recall number: D-634-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,998 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; DOCUSATE SODIUM Capsule, 100 mg may be potentially mislabeled as DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: AD37063_4, EXP: 5/13/2014; tiZANidine HCl, Tablet, 2 mg, NDC 00378072219, Pedigree: W002975, EXP: 6/11/2014.

Code information

DOCUSATE SODIUM, Capsule, 100 mg has the following codes Pedigree: AD37063_1, EXP: 5/13/2014; Pedigree: W002977, EXP: 6/11/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 173 of 273

CRANBERRY Tablet, 450 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 57896084501

D-635-2014

Recall number: D-635-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; CRANBERRY Tablet, 450 mg may be potentially mislabeled as METOPROLOL SUCCINATE ER, Tablet, 200 mg, NDC 62037083301, Pedigree: AD73652_13, EXP: 5/30/2014.

Code information

CRANBERRY, Tablet, 450 mg has the following code Pedigree: AD73640_1, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 174 of 273

SEVELAMER HCl Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 58468002101

D-636-2014

Recall number: D-636-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; SEVELAMER HCl Tablet, 800 mg may be potentially mislabeled as RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: W002857, EXP: 6/7/2014.

Code information

SEVELAMER HCl Tablet, 800 mg has the following code Pedigree: W002858, EXP: 6/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 175 of 273

SEVELAMER CARBONATE Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 58468013001

D-637-2014

Recall number: D-637-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 3,238 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; SEVELAMER CARBONATE Tablet, 800 mg may be potentially mislabeled as tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree: AD46265_16, EXP: 5/15/2014; LEVOTHYROXINE SODIUM, Tablet, 88 mcg, NDC 00781518392, Pedigree: AD70629_13, EXP: 5/29/2014; QUEtiapine FUMARATE, Tablet, 100 mg, NDC 60505313301, Pedigree: W002777, EXP: 6/6/2014; VALSARTAN, Tablet, 160 mg, NDC 0007803

Code information

SEVELAMER CARBONATE, Tablet, 800 mg has the following codes Pedigree: AD39858_4, EXP: 5/15/2014; Pedigree: AD70629_16, EXP: 5/29/2014; Pedigree: W002778, EXP: 6/6/2014; Pedigree: W002859, EXP: 6/7/2014; Pedigree: W003029, EXP: 6/11/2014; Pedigree: AD56917_4, EXP: 5/21/2014; Pedigree: AD73627_11, EXP: 5/30/2014; Pedigree: W002710, EXP: 6/6/2014; Pedigree: W002623, EXP: 6/4/2014; Pedigree: W003491, EXP: 6/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 176 of 273

MULTIVITAMIN/MULTIMINERAL Chew Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 58914001460

D-638-2014

Recall number: D-638-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Chew Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL Chew Tablet may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 12.5 mcg (1/2 of 25 mcg), NDC 00527134101, Pedigree: AD30140_40, EXP: 5/7/2014; LACTOBACILLUS ACIDOPHILUS, Capsule, 500 Million CFU, NDC 43292050022, Pedigree: AD30028_10, EXP: 5/7/2014.

Code information

MULTIVITAMIN/MULTIMINERAL, Chew Tablet has the following codes Pedigree: AD30180_10, EXP: 5/9/2014; Pedigree: AD32325_1, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 177 of 273

ARIPiprazole Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59148000613

D-639-2014

Recall number: D-639-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ARIPiprazole Tablet, 2 mg may be potentially mislabeled as tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree: AD21790_40, EXP: 5/1/2014; ATOMOXETINE HCL, Capsule, 80 mg, NDC 00002325030, Pedigree: AD30140_19, EXP: 5/7/2014; OLANZapine, Tablet, 7.5 mg, NDC 55111016530, Pedigree: AD46265_46, EXP: 5/15/2014; REPAGLINIDE, Tablet, 2 mg, NDC 00169008481, Pedigree: AD464

Code information

ARIPiprazole, Tablet, 2 mg has the following codes Pedigree: AD21790_43, EXP: 5/1/2014; Pedigree: AD30140_25, EXP: 5/7/2014; Pedigree: AD46265_19, EXP: 5/15/2014; Pedigree: AD46414_1, EXP: 5/16/2014; Pedigree: W003004, EXP: 6/11/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 178 of 273

ARIPiprazole Tablet, 15 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59148000913

D-640-2014

Recall number: D-640-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 150 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ARIPiprazole, Tablet, 15 mg may be potentially mislabeled as ATOMOXETINE HCL, Capsule, 40 mg, NDC 00002322930, Pedigree: AD21790_82, EXP: 5/1/2014; PRAMIPEXOLE DI-HCL, Tablet, 0.125 mg, NDC 13668009190, Pedigree: AD25264_10, EXP: 5/3/2014.

Code information

ARIPiprazole Tablet, 15 mg has the following codes Pedigree: AD21965_1, EXP: 5/1/2014; Pedigree: AD28322_1, EXP: 5/6/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 179 of 273

DARUNAVIR Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59676056630

D-641-2014

Recall number: D-641-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; DARUNAVIR Tablet, 800 mg may be potentially mislabeled as HYDROcodone BITARTRATE/ ACETAMINOPHEN, Tablet, 7.5 mg/325 mg, NDC 52544016201, Pedigree: W004005, EXP: 7/1/2014.

Code information

DARUNAVIR, Tablet, 800 mg has the following code Pedigree: W003929, EXP: 7/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 180 of 273

methylPREDNISolone Tablet, 4 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59746000103

D-642-2014

Recall number: D-642-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 21 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; methylPREDNISolone Tablet, 4 mg may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 137 mcg, NDC 00781519192, Pedigree: AD22616_10, EXP: 5/2/2014.

Code information

methylPREDNISolone, Tablet, 4 mg has the following code Pedigree: AD21811_17, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 181 of 273

COLESTIPOL HCL MICRONIZED Tablet, 1 g, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762045001

D-643-2014

Recall number: D-643-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 120 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; COLESTIPOL HCL MICRONIZED Tablet, 1 g may be potentially mislabeled as rifAXIMin, Tablet, 200 mg, NDC 65649030103, Pedigree: AD54587_10, EXP: 4/30/2014.

Code information

COLESTIPOL HCL MICRONIZED, Tablet, 1 g has the following code Pedigree: AD56847_1, EXP: 5/21/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 182 of 273

NIFEdipine Capsule, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762100401

D-644-2014

Recall number: D-644-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; NIFEdipine, Capsule, 10 mg may be potentially mislabeled as NITROFURANTOIN MONOHYDRATE/ MACROCRYSTALS, Capsule, 100 mg, NDC 47781030301, Pedigree: AD52778_58, EXP: 5/20/2014.

Code information

NIFEdipine, Capsule, 10 mg has the following code Pedigree: AD52778_55, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 183 of 273

MIRTAZAPINE Tablet, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762141503

D-645-2014

Recall number: D-645-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 91 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MIRTAZAPINE Tablet, 7.5 mg may be potentially mislabeled as BROMOCRIPTINE MESYLATE, Tablet, 2.5 mg, NDC 00574010603, Pedigree: AD73525_40, EXP: 5/30/2014; DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: W003005, EXP: 6/11/2014; carBAMazepine ER, Tablet, 100 mg, NDC 00078051005, Pedigree: W003330, EXP: 6/18/2014.

Code information

MIRTAZAPINE, Tablet, 7.5 mg has the following codes Pedigree: AD73525_55, EXP: 5/30/2014; Pedigree: W003012, EXP: 6/11/2014; Pedigree: W003334, EXP: 6/18/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 184 of 273

MIRTAZAPINE Tablet, 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762141509

D-646-2014

Recall number: D-646-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MIRTAZAPINE Tablet, 7.5 mg may be potentially mislabeled as ISONIAZID, Tablet, 300 mg, NDC 00555007102, Pedigree: W003691, EXP: 6/26/2014.

Code information

MIRTAZAPINE, Tablet, 7.5 mg has the following code Pedigree: W003693, EXP: 4/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 185 of 273

medroxyPROGESTERone ACETATE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762374202

D-647-2014

Recall number: D-647-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; medroxyPROGESTERone ACETATE, Tablet, 10 mg may be potentially mislabeled as hydrALAZINE HCl, Tablet, 100 mg, NDC 23155000401, Pedigree: AD46312_13, EXP: 5/16/2014.

Code information

medroxyPROGESTERone ACETATE, Tablet, 10 mg has the following code Pedigree: AD46312_19, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 186 of 273

sulfaSALAzine, Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762500001

D-648-2014

Recall number: D-648-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; sulfaSALAzine Tablet, 500 mg may be potentially mislabeled as HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg, NDC 00574025001, Pedigree: AD46265_7, EXP: 5/15/2014.

Code information

sulfaSALAzine, Tablet, 500 mg has the following code Pedigree: AD46265_13, EXP: 5/15/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 187 of 273

MISOPROSTOL, Tablet, 200 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762500801

D-649-2014

Recall number: D-649-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 120 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MISOPROSTOL Tablet, 200 mcg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 10 mg, NDC 23155011001, Pedigree: AD21790_34, EXP: 5/1/2014; SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: W003115, EXP: 6/13/2014.

Code information

MISOPROSTOL, Tablet, 200 mcg has the following codes Pedigree: AD21965_13, EXP: 5/1/2014; Pedigree: W003117, EXP: 6/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 188 of 273

QUINAPRIL HCL Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 59762502001

D-650-2014

Recall number: D-650-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; QUINAPRIL HCL Tablet, 10 mg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 80 mg, NDC 23155011401, Pedigree: AD42566_4, EXP: 5/14/2014.

Code information

QUINAPRIL HCL, Tablet, 10 mg has the following code Pedigree: AD42611_4, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 189 of 273

ZINC SULFATE Capsule, 220 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258013101

D-651-2014

Recall number: D-651-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ZINC SULFATE Capsule, 220 mg may be potentially mislabeled as CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD52778_10, EXP: 5/20/2014; CALCITRIOL, Capsule, 0.25 mcg, NDC 00054000725, Pedigree: W003638, EXP: 6/25/2014.

Code information

ZINC SULFATE, Capsule, 220 mg has the following codes Pedigree: AD52993_34, EXP: 5/20/2014; Pedigree: W003641, EXP: 6/25/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 190 of 273

ASCORBIC ACID Tablet, 500 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258014101

D-652-2014

Recall number: D-652-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ASCORBIC ACID Tablet, 500 mg may be potentially mislabeled as FEBUXOSTAT, Tablet, 40 mg, NDC 64764091830, Pedigree: AD23082_16, EXP: 11/1/2013.

Code information

ASCORBIC ACID Tablet, 500 mg has the following code Pedigree: AD23082_19, EXP: 5/6/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 191 of 273

VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258016001

D-653-2014

Recall number: D-653-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 600 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 88 mcg, NDC 00378180701, Pedigree: AD73652_10, EXP: 5/30/2014; HYOSCYAMINE SULFATE ER, Tablet, 0.375 mg, NDC 43199001401, Pedigree: W003576, EXP: 6/24/2014; MELATONIN, Tablet, 3 mg, NDC 51991001406, Pedigree: AD70655_14, EXP: 5/28/2014; MELATONIN, Tablet, 3 mg, NDC

Code information

VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet has the following codes Pedigree: AD73652_19, EXP: 5/30/2014; Pedigree: W003591, EXP: 6/24/2014; Pedigree: AD70655_17, EXP: 5/28/2014; Pedigree: W003361, EXP: 6/19/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 192 of 273

MAGNESIUM GLUCONATE DIHYDRATE Tablet, 500 mg (27 mg Elemental Magnesium), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258017201

D-654-2014

Recall number: D-654-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MAGNESIUM GLUCONATE DIHYDRATE Tablet, 500 mg (27 mg Elemental Magnesium) may be potentially mislabeled as hydrALAZINE HCl, Tablet, 100 mg, NDC 23155000401, Pedigree: AD30197_7, EXP: 5/9/2014.

Code information

MAGNESIUM GLUCONATE DIHYDRATE, Tablet, 500 mg (27 mg Elemental Magnesium) has the following code Pedigree: AD30197_16, EXP: 5/9/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 193 of 273

CYPROHEPTADINE HCL Tablet, 4 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60258085001

D-655-2014

Recall number: D-655-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 203 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; CYPROHEPTADINE HCL Tablet, 4 mg may be potentially mislabeled as ACARBOSE, Tablet, 25 mg, NDC 00054014025, Pedigree: W003673, EXP: 6/25/2014; AMANTADINE HCL, Capsule, 100 mg, NDC 00781204801, Pedigree: W003323, EXP: 6/18/2014.

Code information

CYPROHEPTADINE HCL, Tablet, 4 mg has the following codes Pedigree: W003676, EXP: 6/25/2014; Pedigree: W003324, EXP: 6/18/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 194 of 273

SENNOSIDES Tablet, 8.6 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 60258095001

D-656-2014

Recall number: D-656-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; SENNOSIDES Tablet, 8.6 mg may be potentially mislabeled as SACCHAROMYCES BOULARDII LYO, Capsule, 250 mg, NDC 00414200007, Pedigree: AD37063_7, EXP: 5/13/2014.

Code information

SENNOSIDES, Tablet, 8.6 mg has the following code Pedigree: AD37063_17, EXP: 5/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 195 of 273

FOSINOPRIL SODIUM Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505251002

D-657-2014

Recall number: D-657-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; FOSINOPRIL SODIUM Tablet, 10 mg may be potentially mislabeled as CALCITRIOL, Capsule, 0.25 mcg, NDC 00054000725, Pedigree: AD46414_10, EXP: 5/16/2014.

Code information

FOSINOPRIL SODIUM, Tablet, 10 mg has the following code Pedigree: AD46414_19, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 196 of 273

FOSINOPRIL SODIUM Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505251102

D-658-2014

Recall number: D-658-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; FOSINOPRIL SODIUM, Tablet, 20 mg may be potentially mislabeled as TOLTERODINE TARTRATE ER, Capsule, 2 mg, NDC 00009519001, Pedigree: AD65478_1, EXP: 5/29/2014.

Code information

FOSINOPRIL SODIUM, Tablet, 20 mg has the following code Pedigree: AD70690_1, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 197 of 273

CILOSTAZOL Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505252201

D-659-2014

Recall number: D-659-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; CILOSTAZOL Tablet, 100 mg may be potentially mislabeled as DUTASTERIDE, Capsule, 0.5 mg, NDC 00173071204, Pedigree: AD65475_1, EXP: 5/28/2014.

Code information

CILOSTAZOL, Tablet, 100 mg has the following code Pedigree: AD65475_4, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 198 of 273

CILOSTAZOL Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505252201

D-660-2014

Recall number: D-660-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; CILOSTAZOL Tablet, 100 mg may be potentially mislabeled as DUTASTERIDE, Capsule, 0.5 mg, NDC 00173071204, Pedigree: AD65475_1, EXP: 5/28/2014.

Code information

CILOSTAZOL Tablet, 100 mg has the following code Pedigree: AD65475_4, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 199 of 273

ATORVASTATIN CALCIUM Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505257909

D-661-2014

Recall number: D-661-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ATORVASTATIN CALCIUM Tablet, 20 mg may be potentially mislabeled as guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003850, EXP: 6/27/2014.

Code information

ATORVASTATIN CALCIUM, Tablet, 20 mg has the following code Pedigree: W003846, EXP: 6/27/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 200 of 273

ATORVASTATIN CALCIUM, Tablet, 80 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505267109

D-662-2014

Recall number: D-662-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ATORVASTATIN CALCIUM, Tablet, 80 mg may be potentially mislabeled as LACTOBACILLUS GG, Capsule, 10 Billion Cells, NDC 49100036374, Pedigree: AD21965_19, EXP: 5/1/2014.

Code information

ATORVASTATIN CALCIUM, Tablet, 80 mg has the following code Pedigree: AD21965_4, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 201 of 273

OLANZAPINE, Tablet 7.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505311203

D-663-2014

Recall number: D-663-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; OLANZAPINE, Tablet 7.5 mg may be potentially mislabeled as NORTRIPTYLINE HCL, Capsule, 75 mg, NDC 00093081301, Pedigree: AD21790_73, EXP: 5/1/2014.

Code information

OLANZAPINE, Tablet, 7.5 mg has the following code Pedigree: AD21790_76, EXP: 5/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 202 of 273

QUEtiapine FUMARATE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505313001

D-664-2014

Recall number: D-664-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 400 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; QUEtiapine FUMARATE, Tablet, 25 mg may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Chew Tablet, NDC 58914001460, Pedigree: AD32325_1, EXP: 5/9/2014; ASPIRIN DR EC, Tablet, 81 mg, NDC 00182106105, Pedigree: W003094, EXP: 6/13/2014.

Code information

QUEtiapine FUMARATE, Tablet, 25 mg has the following codes Pedigree: AD33897_25, EXP: 5/9/2014; Pedigree: W003099, EXP: 6/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 203 of 273

QUEtiapine FUMARATE Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 60505313301

D-665-2014

Recall number: D-665-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; QUEtiapine FUMARATE Tablet, 100 mg may be potentially mislabeled as DOCUSATE CALCIUM, Capsule, 240 mg, NDC 00536375501, Pedigree: W002776, EXP: 6/6/2014; NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 37205098769, Pedigree: W003823, EXP: 6/27/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375710, Pedigree: AD60578_5, EXP: 5/29/2014.

Code information

QUEtiapine FUMARATE, Tablet, 100 mg has the following codes Pedigree: W002777, EXP: 6/6/2014; Pedigree: W003825, EXP: 6/27/2014; Pedigree: AD73623_13, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 204 of 273

ESTERIFIED ESTROGENS Tablet, 0.625 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 61570007301

D-666-2014

Recall number: D-666-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ESTERIFIED ESTROGENS, Tablet, 0.625 mg may be potentially mislabeled as ETODOLAC, Tablet, 400 mg, NDC 51672401801, Pedigree: W003734, EXP: 6/26/2014.

Code information

ESTERIFIED ESTROGENS, Tablet, 0.625 mg has the following code Pedigree: W003736, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 205 of 273

RANOLAZINE ER Tablet, 500 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 61958100301

D-667-2014

Recall number: D-667-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 840 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; RANOLAZINE ER Tablet, 500 mg may be potentially mislabeled as MELATONIN, Tablet, 3 mg, NDC 51991001406, Pedigree: AD25452_16, EXP: 5/3/2014; DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: AD70585_16, EXP: 5/29/2014; OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: W002852, EXP: 6/7/2014; VALSARTAN, Tablet, 80 mg, NDC 00078035834, Pedigree:

Code information

RANOLAZINE ER, Tablet, 500 mg has the following codes Pedigree: AD23087_1, EXP: 5/2/2014; Pedigree: AD62995_7, EXP: 5/29/2014; Pedigree: W002857, EXP: 6/7/2014; Pedigree: W003538, EXP: 6/21/2014; Pedigree: W003741, EXP: 6/26/2014; Pedigree: AD32757_47, EXP: 5/13/2014; Pedigree: W003648, EXP: 6/25/2014; Pedigree: AD60272_40, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 206 of 273

METOPROLOL SUCCINATE ER Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62037083301

D-668-2014

Recall number: D-668-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; METOPROLOL SUCCINATE ER, Tablet, 200 mg may be potentially mislabeled as Pedigree: AD73652_13, EXP: 5/30/2014.

Code information

METOPROLOL SUCCINATE ER Tablet, 200 mg

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 207 of 273

ISOSORBIDE MONONITRATE Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62175010601

D-669-2014

Recall number: D-669-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ISOSORBIDE MONONITRATE Tablet, 10 mg may be potentially mislabeled as ASCORBIC ACID, Tablet, 250 mg, NDC 00904052260, Pedigree: AD28322_10, EXP: 5/6/2014.

Code information

ISOSORBIDE MONONITRATE Tablet, 10 mg has the following code Pedigree: AD28352_1, EXP: 5/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 208 of 273

ISOSORBIDE MONONITRATE, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62175010701

D-670-2014

Recall number: D-670-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ISOSORBIDE MONONITRATE Tablet, 20 mg may be potentially mislabeled as COLCHICINE, Tablet, 0.6 mg, NDC 64764011907, Pedigree: AD52778_22, EXP: 5/20/2014; LOSARTAN POTASSIUM, Tablet, 25 mg, NDC 16714058102, Pedigree: AD67989_7, EXP: 5/28/2014; SODIUM CHLORIDE, Tablet, 1 mg, NDC 00223176001, Pedigree: W002611, EXP: 6/4/2014.

Code information

ISOSORBIDE MONONITRATE, Tablet, 20 mg has the following codes Pedigree: AD52778_31, EXP: 5/20/2014; Pedigree: AD67989_10, EXP: 5/28/2014; Pedigree: W002656, EXP: 6/4/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 209 of 273

ISOSORBIDE MONONITRATE ER Tablet, 30 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62175012837

D-671-2014

Recall number: D-671-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 700 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ISOSORBIDE MONONITRATE ER Tablet, 30 mg may be potentially mislabeled as LOSARTAN POTASSIUM, Tablet, 25 mg, NDC 16714058102, Pedigree: W003899, EXP: 6/27/2014; MISOPROSTOL, Tablet, 100 mcg, NDC 43386016012, Pedigree: AD42611_7, EXP: 5/14/2014; hydrOXYzine PAMOATE, Capsule, 100 mg, NDC 00555032402, Pedigree: W003332, EXP: 6/18/2014; glyBURIDE, Tablet, 2.5 mg, NDC 0009383

Code information

ISOSORBIDE MONONITRATE ER Tablet, 30 mg has the following codes Pedigree: W003996, EXP: 7/1/2014; Pedigree: AD46297_1, EXP: 5/15/2014; Pedigree: W003350, EXP: 6/18/2014; Pedigree: AD21790_64, EXP: 5/1/2014; Pedigree: AD32757_37, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 210 of 273

PANTOPRAZOLE SODIUM DR Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62175018046

D-672-2014

Recall number: D-672-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; PANTOPRAZOLE SODIUM DR, Tablet, 20 mg may be potentially mislabeled as DRONEDARONE HCL, Tablet, 400 mg, NDC 00024414260, Pedigree: AD52778_52, EXP: 5/20/2014.

Code information

PANTOPRAZOLE SODIUM DR Tablet, 20 mg has the following code Pedigree: AD52778_64, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 211 of 273

OXcarbazepine Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018388

D-673-2014

Recall number: D-673-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; OXcarbazepine Tablet, 150 mg may be potentially mislabeled as traZODone HCl, Tablet, 50 mg, NDC 50111043301, Pedigree: AD54562_1, EXP: 5/20/2014.

Code information

OXcarbazepine, Tablet, 150 mg has the following code Pedigree: AD54562_4, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 212 of 273

OXcarbazepine Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756018588

D-674-2014

Recall number: D-674-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; OXcarbazepine Tablet, 600 mg may be potentially mislabeled as LACTASE ENZYME, Tablet, 3000 units, NDC 24385014976, Pedigree: AD30028_25, EXP: 5/7/2014.

Code information

OXcarbazepine, Tablet, 600 mg has the following code Pedigree: AD30140_46, EXP: 5/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 213 of 273

LETROZOLE Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 62756051183

D-675-2014

Recall number: D-675-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; LETROZOLE Tablet, 2.5 mg may be potentially mislabeled as METOPROLOL TARTRATE, Tablet, 50 mg, NDC 00093073301, Pedigree: W003848, EXP: 6/27/2014.

Code information

LETROZOLE, Tablet, 2.5 mg has the following code Pedigree: W003868, EXP: 6/27/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 214 of 273

CALCITRIOL Capsule, 0.5 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63304024001

D-676-2014

Recall number: D-676-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 500 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; CALCITRIOL, Capsule, 0.5 mcg may be potentially mislabeled as NIACIN TR, Tablet, 250 mg, NDC 10939043533, Pedigree: W003756, EXP: 5/31/2014; ISONIAZID, Tablet, 300 mg, NDC 00555007102, Pedigree: AD32757_28, EXP: 5/13/2014.

Code information

CALCITRIOL, Capsule, 0.5 mcg has the following codes Pedigree: W003730, EXP: 6/26/2014; Pedigree: AD32757_10, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 215 of 273

HYDROXYCHLOROQUINE SULFATE Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63304029601

D-677-2014

Recall number: D-677-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; HYDROXYCHLOROQUINE SULFATE, Tablet, 200 mg may be potentially mislabeled as guanFACINE HCl, Tablet, 1 mg, NDC 00378116001, Pedigree: AD70629_7, EXP: 5/29/2014.

Code information

HYDROXYCHLOROQUINE SULFATE, Tablet, 200 mg has the following code Pedigree: AD70629_10, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 216 of 273

METOPROLOL TARTRATE Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 63304057901

D-678-2014

Recall number: D-678-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 420 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; METOPROLOL TARTRATE, Tablet, 12.5 mg (1/2 of 25 mg) may be potentially mislabeled as PIOGLITAZONE, Tablet, 15 mg, NDC 00591320530, Pedigree: AD22845_1, EXP: 4/30/2014; LEVOTHYROXINE SODIUM, Tablet, 12.5 mcg (1/2 of 25 mcg), NDC 00527134101, Pedigree: AD73525_49, EXP: 5/30/2014.

Code information

METOPROLOL TARTRATE, Tablet, 12.5 mg (1/2 of 25 mg) has the following codes Pedigree: AD21790_67, EXP: 5/1/2014; Pedigree: AD73525_52, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 217 of 273

ATENOLOL Tablet, 12.5 mg (1/2 of 25 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 63304062101

D-679-2014

Recall number: D-679-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 398 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ATENOLOL, Tablet, 12.5 mg (1/2 of 25 mg) may be potentially mislabeled as VITAMIN B COMPLEX WITH C/FOLIC ACID, Tablet, NDC 60258016001, Pedigree: AD73652_19, EXP: 5/30/2014; PIROXICAM, Capsule, 10 mg, NDC 00093075601, Pedigree: AD21836_1, EXP: 3/31/2014.

Code information

ATENOLOL, Tablet, 12.5 mg (1/2 of 25 mg) has the following codes Pedigree: AD73525_1, EXP: 5/30/2014; Pedigree: AD30140_1, EXP: 5/7/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 218 of 273

ESZOPICLONE, Tablet, 3 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63402019310

D-680-2014

Recall number: D-680-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; ESZOPICLONE, Tablet, 3 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 1000 units, NDC 00904582460, Pedigree: W002779, EXP: 6/6/2014.

Code information

ESZOPICLONE, Tablet, 3 mg has the following code Pedigree: W002765, EXP: 6/6/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 219 of 273

LURASIDONE HCL, Tablet, 120 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63402031230

D-681-2014

Recall number: D-681-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; LURASIDONE HCl Tablet, 120 mg may be potentially mislabeled as DULoxetine HCl DR, Capsule, 20 mg, NDC 00002323560, Pedigree: W003486, EXP: 6/20/2014.

Code information

LURASIDONE HCL, Tablet, 120 mg has the following code Pedigree: W003487, EXP: 6/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 220 of 273

guaiFENesin ER, Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000815

D-682-2014

Recall number: D-682-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 600 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; guaiFENesin ER, Tablet, 600 mg may be potentially mislabeled as MISOPROSTOL, Tablet, 200 mcg, NDC 59762500801, Pedigree: AD21965_13, EXP: 5/1/2014; TACROLIMUS, Capsule, 1 mg, NDC 00781210301, Pedigree: AD56917_7, EXP: 5/21/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: AD73627_17, EXP: 5/30/2014; LACTOBACILLUS GG, Capsule, NDC 49100036374, Pedigree: W003216

Code information

guaiFENesin ER, Tablet, 600 mg has the following codes Pedigree: AD21965_22, EXP: 5/1/2014; Pedigree: AD56917_13, EXP: 5/21/2014; Pedigree: AD73627_23, EXP: 5/30/2014; Pedigree: W003218, EXP: 6/17/2014; Pedigree: W003360, EXP: 6/19/2014; Pedigree: W002660, EXP: 6/5/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 221 of 273

guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000834

D-683-2014

Recall number: D-683-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 480 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; guaiFENesin ER, Tablet, 600 mg may be potentially mislabeled as PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet, NDC 51991056601, Pedigree: AD62829_18, EXP: 5/24/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: AD62834_4, EXP: 5/24/2014; diphenhydrAMINE HCl, Tablet, 25 mg, NDC 00904555159, Pedigree: W003513, EXP: 6/21/2014; DOCUSATE SODIUM, Capsule, 250 mg,

Code information

guaiFENesin ER, Tablet, 600 mg has the following codes Pedigree: AD62834_4, EXP: 5/24/2014; Pedigree: AD62834_7, EXP: 5/24/2014; Pedigree: W003514, EXP: 6/21/2014; Pedigree: W003574, EXP: 6/24/2014; Pedigree: W003850, EXP: 6/27/2014; Pedigree: W003931, EXP: 6/28/2014; Pedigree: AD46429_1, EXP: 5/15/2014; Pedigree: AD73592_1, EXP: 5/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 222 of 273

guaiFENesin ER Tablet, 600 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824000850

D-684-2014

Recall number: D-684-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 500 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; guaiFENesin ER Tablet, 600 mg may be potentially mislabeled as OMEGA-3-ACID ETHYL ESTERS, Capsule, 1000 mg, NDC 00173078302, Pedigree: W003243, EXP: 6/17/2014.

Code information

guaiFENesin ER, Tablet, 600 mg has the following code Pedigree: W003244, EXP: 6/17/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 223 of 273

BENZOCAINE/MENTHOL Lozenge, 15 mg/3.6 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824072016

D-685-2014

Recall number: D-685-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 80 Lozenges

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; BENZOCAINE/MENTHOL Lozenge, 15 mg/3.6 mg may be potentially mislabeled as LUBIPROSTONE, Capsule, 24 mcg, NDC 64764024060, Pedigree: AD21811_1, EXP: 5/1/2014; LOSARTAN POTASSIUM, Tablet, 50 mg, NDC 00093736598, Pedigree: W003268, EXP: 6/17/2014.

Code information

BENZOCAINE/MENTHOL, Lozenge, 15 mg/3.6 mg has the following codes Pedigree: AD21811_4, EXP: 5/1/2014; Pedigree: W003273, EXP: 6/17/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 224 of 273

BENZOCAINE/MENTHOL, Lozenge, 15 mg/2.6 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 63824073116

D-686-2014

Recall number: D-686-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 32 Lozenges

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; BENZOCAINE/MENTHOL Lozenge, 15 mg/2.6 mg may be potentially mislabeled as CHOLECALCIFEROL/ CALCIUM/ PHOSPHORUS, Tablet, 120 units/105 mg/81 mg, NDC 64980015001, Pedigree: AD32345_1, EXP: 5/14/2014.

Code information

BENZOCAINE/MENTHOL, Lozenge, 15 mg/2.6 mg has the following code Pedigree: AD42592_4, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 225 of 273

MULTIVITAMIN/MULTIMINERAL W/FLUORIDE, Chew Tablet, 1 mg (F), Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64376081501

D-687-2014

Recall number: D-687-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Chew Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL W/FLUORIDE, Chew Tablet, 1 mg (F) may be potentially mislabeled as ISOMETHEPTENE MUCATE/ DICHLORALPHENAZONE/APAP, Capsule, 65 mg/100 mg/325 mg, NDC 44183044001, Pedigree: AD22858_1, EXP: 3/31/2014.

Code information

MULTIVITAMIN/MULTIMINERAL W/FLUORIDE, Chew Tablet, 1 mg (F) has the following code Pedigree: AD22609_7, EXP: 5/2/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 226 of 273

MULTIVITAMIN/MULTIMINERAL LOW IRON Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64376081601

D-688-2014

Recall number: D-688-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 400 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL LOW IRON Tablet may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 112 mcg, NDC 00527134601, Pedigree: AD60272_22, EXP: 5/22/2014; ATORVASTATIN CALCIUM, Tablet, 80 mg, NDC 00378212277, Pedigree: AD73627_1, EXP: 5/30/2014; MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 37205018581, Pedigree: W002513, EXP: 6/3/2014.

Code information

MULTIVITAMIN/MULTIMINERAL LOW IRON Tablet has the following codes Pedigree: AD60272_31, EXP: 5/22/2014; Pedigree: AD73627_8, EXP: 5/30/2014; Pedigree: W002507, EXP: 6/3/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 227 of 273

PANTOPRAZOLE SODIUM DR Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679043304

D-689-2014

Recall number: D-689-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; PANTOPRAZOLE SODIUM DR Tablet, 20 mg may be potentially mislabeled as FOSINOPRIL SODIUM, Tablet, 20 mg, NDC 60505251102, Pedigree: AD70690_1, EXP: 5/29/2014.

Code information

PANTOPRAZOLE SODIUM DR Tablet, 20 mg has the following codes Pedigree: AD70690_4, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 228 of 273

PANTOPRAZOLE SODIUM DR Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679043402

D-690-2014

Recall number: D-690-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,001 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; PANTOPRAZOLE SODIUM DR Tablet, 40 mg may be potentially mislabeled as SENNOSIDES, Tablet, 8.6 mg, NDC 60258095001, Pedigree: AD37063_17, EXP: 5/13/2014.

Code information

PANTOPRAZOLE SODIUM DR Tablet, 40 mg has the following code Pedigree: AD37063_10, EXP: 5/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 229 of 273

ZOLPIDEM TARTRATE, Tablet, 2.5 mg (1/2 of 5 mg), Rx only, Distributed by: AidaPak Service, LLC, NDC 64679071401

D-691-2014

Recall number: D-691-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 402 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ZOLPIDEM TARTRATE Tablet, 2.5 mg (1/2 of 5 mg) may be potentially mislabeled as TEMAZEPAM, Capsule, 7.5 mg, NDC 00378311001, Pedigree: AD22861_7, EXP: 5/8/2014.

Code information

ZOLPIDEM TARTRATE Tablet, 2.5 mg (1/2 of 5 mg) has the following code Pedigree: AD28355_1, EXP: 5/8/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 230 of 273

LISINOPRIL Tablet, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679092701

D-692-2014

Recall number: D-692-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LISINOPRIL Tablet, 2.5 mg may be potentially mislabeled as RANOLAZINE ER, Tablet, 500 mg, NDC 61958100301, Pedigree: AD23087_1, EXP: 5/2/2014; DOCUSATE SODIUM, Capsule, 250 mg, NDC 00536375701, Pedigree: W003358, EXP: 6/19/2014.

Code information

LISINOPRIL Tablet, 2.5 mg has the following codes Pedigree: AD25264_4, EXP: 5/3/2014; Pedigree: W003365, EXP: 6/19/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 231 of 273

ZONISAMIDE Capsule, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64679099001

D-693-2014

Recall number: D-693-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; ZONISAMIDE Capsule, 100 mg may be potentially mislabeled as PHYTONADIONE, Tablet, 5 mg, NDC 25010040515, Pedigree: W003737, EXP: 5/31/2014.

Code information

ZONISAMIDE Capsule, 100 mg has the following code Pedigree: W003786, EXP: 6/27/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 232 of 273

METAXALONE Tablet, 800 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64720032110

D-694-2014

Recall number: D-694-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; METAXALONE Tablet, 800 mg may be potentially mislabeled as ESTERIFIED ESTROGENS, Tablet, 0.625 mg, NDC 61570007301, Pedigree: W003736, EXP: 6/26/2014.

Code information

METAXALONE Tablet, 800 mg has the following code Pedigree: W003738, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 233 of 273

HYDROCORTISONE Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64720033105

D-695-2014

Recall number: D-695-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; HYDROCORTISONE Tablet, 5 mg may be potentially mislabeled as ORPHENADRINE CITRATE ER, Tablet, 100 mg, NDC 43386048024, Pedigree: W002962, EXP: 6/11/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: W003045, EXP: 6/12/2014.

Code information

HYDROCORTISONE Tablet, 5 mg has the following codes Pedigree: W002966, EXP: 6/11/2014; Pedigree: W003046, EXP: 6/12/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 234 of 273

COLCHICINE Tablet, 0.6 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64764011907

D-696-2014

Recall number: D-696-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 150 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; COLCHICINE Tablet, 0.6 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 2000 units, NDC 00904615760, Pedigree: AD46312_37, EXP: 5/16/2014; PSEUDOEPHEDRINE HCL, Tablet, 30 mg, NDC 00904505360, Pedigree: AD52993_37, EXP: 5/20/2014; SENNOSIDES, Tablet, 8.6 mg, NDC 00182109301, Pedigree: AD62992_14, EXP: 5/23/2014; CHOLECALCIFEROL, Tablet, 1000 units, NDC 00904

Code information

COLCHICINE Tablet, 0.6 mg has the following codes Pedigree: AD46419_1, EXP: 5/16/2014; Pedigree: AD52778_22, EXP: 5/20/2014; Pedigree: AD65457_1, EXP: 5/23/2014; Pedigree: W003612, EXP: 6/25/2014; Pedigree: W002961, EXP: 6/11/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 235 of 273

LUBIPROSTONE Capsule, 24 mcg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64764024060

D-697-2014

Recall number: D-697-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LUBIPROSTONE Capsule, 24 mcg may be potentially mislabeled as ARIPiprazole, Tablet, 2 mg, NDC 59148000613, Pedigree: AD21790_43, EXP: 5/1/2014; CYANOCOBALAMIN, Tablet, 1000 mcg, NDC 00904421713, Pedigree: AD21846_46, EXP: 5/1/2014; VALSARTAN, Tablet, 160 mg, NDC 00078035934, Pedigree: AD39858_1, EXP: 5/16/2014.

Code information

LUBIPROSTONE Capsule, 24 mcg has the following codes Pedigree: AD21790_46, EXP: 5/1/2014; Pedigree: AD21811_1, EXP: 5/1/2014; Pedigree: AD46312_1, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 236 of 273

FEBUXOSTAT Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64764091830

D-698-2014

Recall number: D-698-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 300 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; FEBUXOSTAT Tablet, 40 mg may be potentially mislabeled as methylPREDNISolone, Tablet, 4 mg, NDC 59746000103, Pedigree: AD21811_17, EXP: 5/1/2014; tiZANidine HCl, Tablet, 2 mg, NDC 55111017915, Pedigree: W002663, EXP: 6/5/2014; SODIUM CHLORIDE, Tablet, 1000 mg, NDC 00527111610, Pedigree: W003926, EXP: 7/1/2014.

Code information

FEBUXOSTAT Tablet, 40 mg has the following codes Pedigree: AD23082_16, EXP: 11/1/2013; Pedigree: W002664, EXP: 6/5/2014; Pedigree: W003927, EXP: 7/1/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 237 of 273

PHOSPHORUS Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980010401

D-699-2014

Recall number: D-699-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,000 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; PHOSPHORUS Tablet, 250 mg may be potentially mislabeled as CITALOPRAM, Tablet, 10 mg, NDC 57664050788, Pedigree: AD56921_1, EXP: 5/21/2014; VENLAFAXINE HCL, Tablet, 75 mg, NDC 00093738201, Pedigree: W002533, EXP: 2/28/2014; NITROFURANTOIN MACROCRYSTALS, Capsule, 50 mg, NDC 47781030701, Pedigree: AD25452_4, EXP: 5/3/2014; traZODone HCl, Tablet, 50 mg, NDC 50111043303, P

Code information

PHOSPHORUS Tablet, 250 mg has the following codes Pedigree: AD56916_1, EXP: 5/21/2014; Pedigree: W002534, EXP: 6/3/2014; Pedigree: AD25452_7, EXP: 5/3/2014; Pedigree: AD54498_1, EXP: 5/20/2014; Pedigree: W003997, EXP: 7/1/2014; Pedigree: AD46300_8, EXP: 5/15/2014; Pedigree: AD70639_10, EXP: 5/29/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 238 of 273

LACTOBACILLUS Tablet, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980012950

D-700-2014

Recall number: D-700-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,249 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; LACTOBACILLUS Tablet may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 65162066850, Pedigree: AD62979_1, EXP: 5/23/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD62986_1, EXP: 5/23/2014; LITHIUM CARBONATE ER, Tablet, 225 mg (1/2 of 450 mg), NDC 00054002025, Pedigree: AD21790_25, EXP: 5/1/2014; OMEGA-3 FATTY ACID, Capsule, 100

Code information

LACTOBACILLUS Tablet has the following codes Pedigree: AD62986_10, EXP: 5/23/2014; Pedigree: AD62992_1, EXP: 5/23/2014; Pedigree: AD22865_1, EXP: 5/2/2014; Pedigree: W003624, EXP: 1/31/2014; Pedigree: W003622, EXP: 6/25/2014; Pedigree: W003623, EXP: 10/31/2013.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 239 of 273

CHOLECALCIFEROL/ CALCIUM/ PHOSPHORUS Tablet, 120 units/105 mg/81 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980015001

D-701-2014

Recall number: D-701-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 509 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; CHOLECALCIFEROL/CALCIUM/PHOSPHORUS Tablet, 120 units/105 mg/81 mg may be potentially mislabeled as PROMETHAZINE HCL, Tablet, 25 mg, NDC 65162052110, Pedigree: W002578, EXP: 6/3/2014; VALSARTAN, Tablet, 40 mg, NDC 00078042315, Pedigree: AD32579_1, EXP: 5/9/2014.

Code information

CHOLECALCIFEROL/CALCIUM/PHOSPHORUS Tablet, 120 units/105 mg/81 mg has the following codes Pedigree: W002581, EXP: 6/3/2014; Pedigree: AD32345_1, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 240 of 273

aMILoride HCl Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980015101

D-702-2014

Recall number: D-702-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; aMILoride HCl Tablet, 5 mg may be potentially mislabeled as PROPRANOLOL HCL, Tablet, 10 mg, NDC 23155011001, Pedigree: AD60272_37, EXP: 5/22/2014; FAMOTIDINE, Tablet, 20 mg, NDC 16714036104, Pedigree: W003764, EXP: 6/26/2014.

Code information

aMILoride HC, Tablet, 5 mg has the following codes Pedigree: AD60272_55, EXP: 5/22/2014; Pedigree: W003686, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 241 of 273

DISULFIRAM Tablet, 250 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980017101

D-703-2014

Recall number: D-703-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; DISULFIRAM Tablet, 250 mg may be potentially mislabeled as PYRIDOXINE HCL, Tablet, 50 mg, NDC 00904052060, Pedigree: AD22865_22, EXP: 5/2/2014.

Code information

DISULFIRAM Tablet, 250 mg has the following code Pedigree: AD22609_1, EXP: 5/2/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 242 of 273

SODIUM BICARBONATE Tablet, 650 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 64980018210

D-704-2014

Recall number: D-704-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,013 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; SODIUM BICARBONATE Tablet, 650 mg may be potentially mislabeled as NICOTINE POLACRILEX, Lozenge, 2 mg, NDC 00135051001, Pedigree: W002974, EXP: 6/11/2014.

Code information

SODIUM BICARBONATE Tablet, 650 mg has the following code Pedigree: W002970, EXP: 6/11/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 243 of 273

RILUZOLE Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 64980019106

D-705-2014

Recall number: D-705-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 240 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; RILUZOLE Tablet, 50 mg may be potentially mislabeled as traZODone HCl, Tablet, 150 mg, NDC 50111044101, Pedigree: W003245, EXP: 6/17/2014.

Code information

RILUZOLE Tablet, 50 mg has the following code Pedigree: W003255, EXP: 6/17/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 244 of 273

FOLIC ACID, Tablet, 1 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162036110

D-706-2014

Recall number: D-706-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,000 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; FOLIC ACID, Tablet, 1 mg may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: AD32328_5, EXP: 5/9/2014; DOCUSATE CALCIUM, Capsule, 240 mg, NDC 00536375501, Pedigree: W003821, EXP: 6/27/2014; ATORVASTATIN CALCIUM, Tablet, 40 mg, NDC 00378212177, Pedigree: W003096, EXP: 6/13/2014.

Code information

FOLIC ACID, Tablet, 1 mg has the following codes Pedigree: AD33897_22, EXP: 5/9/2014; Pedigree: W003822, EXP: 6/27/2014; Pedigree: W003097, EXP: 6/13/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 245 of 273

PROMETHAZINE HCL, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162052110

D-707-2014

Recall number: D-707-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; PROMETHAZINE HCL, Tablet, 25 mg may be potentially mislabeled as CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: W002574, EXP: 6/3/2014.

Code information

PROMETHAZINE HCL, Tablet, 25 mg has the following code Pedigree: W002578, EXP: 6/3/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 246 of 273

FLECAINIDE ACETATE Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162064110

D-708-2014

Recall number: D-708-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; FLECAINIDE ACETATE Tablet, 50 mg may be potentially mislabeled as VITAMIN B COMPLEX W/C, Tablet, NDC 00904026013, Pedigree: AD46419_7, EXP: 5/16/2014.

Code information

FLECAINIDE ACETATE Tablet, 50 mg has the following code Pedigree: AD46414_16, EXP: 5/16/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 247 of 273

MULTIVITAMIN/MULTIMINERAL Tablet, Distributed by: AidaPak Service, LLC, NDC 65162066810

D-709-2014

Recall number: D-709-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL Tablet may be potentially mislabeled as PRENATAL MULTIVITAMIN/MULTIMINERAL Tablet, NDC 00904531360, Pedigree: AD73652_16, EXP: 5/30/2014.

Code information

MULTIVITAMIN/MULTIMINERAL Tablet has the following code Pedigree: AD73646_13, EXP: 5/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 248 of 273

MULTIVITAMIN/MULTIMINERAL Tablet, Distributed by: AidaPak Service, LLC, NDC 65162066850

D-710-2014

Recall number: D-710-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 1,000 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MULTIVITAMIN/MULTIMINERAL Tablet may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 00904404360, Pedigree: AD62865_13, EXP: 5/23/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003514, EXP: 6/21/2014.

Code information

MULTIVITAMIN/MULTIMINERAL Tablet has the following codes Pedigree: AD62979_1, EXP: 5/23/2014; Pedigree: W003553, EXP: 6/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 249 of 273

guanFACINE HCl Tablet, 2 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162071310

D-711-2014

Recall number: D-711-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 501 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; guanFACINE HCl Tablet, 2 mg may be potentially mislabeled as buPROPion HCl ER, Tablet, 200 mg, NDC 47335073886, Pedigree: AD21790_4, EXP: 5/1/2014; AMANTADINE HCL, Capsule, 100 mg, NDC 00781204801, Pedigree: W002997, EXP: 6/11/2014; glyBURIDE, Tablet, 1.25 mg, NDC 00093834201, Pedigree: W003677, EXP: 2/28/2014; ACYCLOVIR, Capsule, 200 mg, NDC 00093894001, Pedigree: AD60

Code information

guanFACINE HCl Tablet, 2 mg has the following codes Pedigree: AD21790_13, EXP: 5/1/2014; Pedigree: W002999, EXP: 6/11/2014; Pedigree: W003678, EXP: 6/25/2014; Pedigree: AD60272_10, EXP: 5/22/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 250 of 273

BENAZEPRIL HCL Tablet, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075110

D-712-2014

Recall number: D-712-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 5 mg may be potentially mislabeled as ZINC SULFATE, Capsule, 220 mg, NDC 60258013101, Pedigree: AD52993_34, EXP: 5/20/2014.

Code information

BENAZEPRIL HCL Tablet, 5 mg has the following code Pedigree: AD52778_7, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 251 of 273

BENAZEPRIL HCL Tablet, 40 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65162075410

D-713-2014

Recall number: D-713-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 799 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; BENAZEPRIL HCL Tablet, 40 mg may be potentially mislabeled as NEFAZODONE HCL, Tablet, 200 mg, NDC 00093102506, Pedigree: AD46414_44, EXP: 5/16/2014; guaiFENesin ER, Tablet, 600 mg, NDC 63824000834, Pedigree: W003931, EXP: 6/28/2014; CALCIUM ACETATE, Capsule, 667 mg, NDC 00054008826, Pedigree: AD42592_1, EXP: 5/14/2014; ACETAMINOPHEN/ ASPIRIN/ CAFFEINE, Tablet, 250 mg/25

Code information

BENAZEPRIL HCL Tablet, 40 mg has the following codes Pedigree: AD49423_1, EXP: 5/16/2014; Pedigree: W003918, EXP: 6/28/2014; Pedigree: AD32757_7, EXP: 5/13/2014; Pedigree: AD68010_1, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 252 of 273

COLESEVELAM HCL Tablet, 625 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65597070118

D-714-2014

Recall number: D-714-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 180 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; COLESEVELAM HCL Tablet, 625 mg may be potentially mislabeled as lamoTRIgine Tablet, 50 mg (1/2 of 100 mg), NDC 13668004701, Pedigree: AD46265_31, EXP: 5/15/2014.

Code information

COLESEVELAM HCL Tablet, 625 mg has the following code Pedigree: AD46426_19, EXP: 5/15/2014

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 253 of 273

rifAXIMin Tablet, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65649030103

D-715-2014

Recall number: D-715-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; rifAXIMin Tablet, 200 mg may be potentially mislabeled as CapsuleTOPRIL, Tablet, 25 mg, NDC 00143117201, Pedigree: AD52778_19, EXP: 5/20/2014.

Code information

rifAXIMin Tablet, 200 mg has the following code Pedigree: AD54587_10, EXP: 4/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 254 of 273

QUEtiapine FUMARATE, Tablet, 25 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65862048901

D-716-2014

Recall number: D-716-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 400 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; QUEtiapine FUMARATE, Tablet, 25 mg may be potentially mislabeled as chlordiazePOXIDE HCl, Capsule, 25 mg, NDC 00555015902, Pedigree: AD49426_1, EXP: 5/16/2014.

Code information

QUEtiapine FUMARATE, Tablet, 25 mg has the following code Pedigree: AD49582_22, EXP: 4/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 255 of 273

IRBESARTAN, Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 65862063830

D-717-2014

Recall number: D-717-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; IRBESARTAN, Tablet, 150 mg may be potentially mislabeled as ATROPINE SULFATE/DIPHENOXYLATE HCL, Tablet, 0.025 mg/2.5 mg, NDC 00378041501, Pedigree: W003597, EXP: 6/24/2014; CHOLECALCIFEROL, Tablet, 400 units, NDC 00904582360, Pedigree: AD76686_7, EXP: 5/31/2014.

Code information

IRBESARTAN, Tablet, 150 mg has the following codes Pedigree: W003649, EXP: 6/25/2014; Pedigree: AD73686_7, EXP: 5/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 256 of 273

PHENobarbital/ HYOSCYAMINE/ ATROPINE/ SCOPOLAMINE, Tablet, 16.2 mg/0.1037 mg/0.0194 mg/0.0065 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 66213042510

D-718-2014

Recall number: D-718-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; PHENobarbital/ HYOSCYAMINE/ ATROPINE/ SCOPOLAMINE, Tablet, 16.2 mg/0.1037 mg/0.0194 mg/0.0065 mg may be potentially mislabeled as VALSARTAN, Tablet, 160 mg, NDC 00078035934, Pedigree: W003639, EXP: 6/25/2014.

Code information

PHENobarbital/ HYOSCYAMINE/ ATROPINE/ SCOPOLAMINE, Tablet, 16.2 mg/0.1037 mg/0.0194 mg/0.0065 mg has the following code Pedigree: W003640, EXP: 6/25/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 257 of 273

carBAMazepine ER, Capsule, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 66993040832

D-719-2014

Recall number: D-719-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 229 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; carBAMazepine ER, Capsule, 200 mg may be potentially mislabeled as ACAMPROSATE CALCIUM DR, Tablet, 333 mg, NDC 00456333001, Pedigree: AD46333_1, EXP: 5/15/2014.

Code information

carBAMazepine ER, Capsule, 200 mg has the following code Pedigree: AD32764_14, EXP: 5/14/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 258 of 273

SELEGILINE HCL, Capsule, 5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 67253070006

D-720-2014

Recall number: D-720-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; SELEGILINE HCL, Capsule, 5 mg may be potentially mislabeled as ITRACONAZOLE, Capsule, 100 mg, NDC 10147170003, Pedigree: AD54549_10, EXP: 5/20/2014.

Code information

SELEGILINE HCL, Capsule, 5 mg has the following code Pedigree: AD54549_19, EXP: 5/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 259 of 273

DOCUSATE SODIUM, Capsule, 50 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 67618010060

D-721-2014

Recall number: D-721-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 181 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; DOCUSATE SODIUM, Capsule, 50 mg may be potentially mislabeled as LEVOTHYROXINE SODIUM, Tablet, 112 mcg, NDC 00378181101, Pedigree: AD60211_1, EXP: 5/21/2014; MEXILETINE HCL, Capsule, 150 mg, NDC 00093873901, Pedigree: AD62865_7, EXP: 5/23/2014; CHOLECALCIFEROL, Tablet, 5000 units, NDC 00761017840, Pedigree: AD65457_10, EXP: 5/24/2014.

Code information

DOCUSATE SODIUM, Capsule, 50 mg has the following codes Pedigree: AD60211_8, EXP: 5/21/2014; Pedigree: AD62865_10, EXP: 5/23/2014; Pedigree: AD65457_13, EXP: 5/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 260 of 273

buPROPion HCl ER (XL), Tablet, 150 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 67767014130

D-722-2014

Recall number: D-722-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 60 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; buPROPion HCl ER (XL), Tablet, 150 mg may be potentially mislabeled as MESALAMINE CR, Capsule, 250 mg, NDC 54092018981, Pedigree: AD52412_1, EXP: 5/17/2014.

Code information

buPROPion HCl ER (XL), Tablet, 150 mg has the following code Pedigree: AD52412_4, EXP: 4/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 261 of 273

IBUPROFEN, Tablet, 400 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 67877029401

D-723-2014

Recall number: D-723-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; IBUPROFEN, Tablet, 400 mg may be potentially mislabeled as ASPIRIN, Tablet, 325 mg, NDC 00536330501, Pedigree: W002573, EXP: 6/3/2014.

Code information

IBUPROFEN, Tablet, 400 mg has the following code Pedigree: W002577, EXP: 6/3/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 262 of 273

QUINAPRIL HCL, Tablet, 20 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68180055809

D-724-2014

Recall number: D-724-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; QUINAPRIL HCL, Tablet, 20 mg may be potentially mislabeled as MULTIVITAMIN/MULTIMINERAL, Tablet, NDC 65162066850, Pedigree: W003553, EXP: 6/24/2014.

Code information

QUINAPRIL HCL, Tablet, 20 mg has the following code Pedigree: W003556, EXP: 6/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 263 of 273

RAMIPRIL, Capsule, 2.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68180058901

D-725-2014

Recall number: D-725-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; RAMIPRIL, Capsule, 2.5 mg, Rx only may be potentially mislabeled as PROPAFENONE HCL, Tablet, 150 mg, NDC 00591058201, Pedigree: AD54549_13, EXP: 5/20/2014; CALCIUM POLYCARBOPHIL, Tablet, 625 mg, NDC 00536430611, Pedigree: AD73592_11, EXP: 5/31/2014.

Code information

RAMIPRIL, Capsule, 2.5 mg, Rx only has the following codes Pedigree: AD54549_16, EXP: 5/20/2014; Pedigree: AD76639_1, EXP: 5/31/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 264 of 273

amLODIPine BESYLATE, Tablet, 10 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68382012316

D-726-2014

Recall number: D-726-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; amLODIPine BESYLATE, Tablet, 10 mg may be potentially mislabeled as FINASTERIDE, Tablet, 5 mg, NDC 16714052201, Pedigree: AD62846_1, EXP: 2/28/2014.

Code information

amLODIPine BESYLATE, Tablet, 10 mg has the following code Pedigree: AD62846_4, EXP: 5/24/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 265 of 273

RIBAVIRIN, Capsule, 200 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68382026007

D-727-2014

Recall number: D-727-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 168 Capsules

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; RIBAVIRIN, Capsule, 200 mg may be potentially mislabeled as MODAFINIL, Tablet, 50 mg (1/2 of 100 MG Tablet), NDC 55253080130, Pedigree: AD21787_4, EXP: 5/1/2014; DESIPRAMINE HCL, Tablet, 50 mg, NDC 45963034302, Pedigree: AD30140_7, EXP: 5/7/2014.

Code information

RIBAVIRIN, Capsule, 200 mg has the following codes Pedigree: AD21790_37, EXP: 4/30/2014; Pedigree: AD30140_13, EXP: 4/30/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 266 of 273

FLUCONAZOLE, Tablet, 50 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68462010130

D-728-2014

Recall number: D-728-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 29 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; FLUCONAZOLE, Tablet, 50 mg may be potentially mislabeled as FLUCONAZOLE, Tablet, 200 mg, NDC 00172541360, Pedigree: W003065, EXP: 6/12/2014.

Code information

FLUCONAZOLE, Tablet, 50 mg has the following code Pedigree: W003066, EXP: 6/12/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 267 of 273

FLUCONAZOLE, Tablet, 100 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68462010230

D-729-2014

Recall number: D-729-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; FLUCONAZOLE, Tablet, 100 mg may be potentially mislabeled as PRENATAL MULTIVITAMIN/ MULTIMINERAL, Tablet, NDC 51991056601, Pedigree: W003086, EXP: 6/12/2014.

Code information

FLUCONAZOLE, Tablet, 100 mg has the following code Pedigree: W003064, EXP: 6/12/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 268 of 273

VERAPAMIL HCL ER, Tablet, 240 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68462026001

D-730-2014

Recall number: D-730-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 100 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; VERAPAMIL HCL ER, Tablet, 240 mg may be potentially mislabeled as TRIFLUOPERAZINE HCL, Tablet, 1 mg, NDC 00781103001, Pedigree: AD52778_91, EXP: 5/21/2014.

Code information

VERAPAMIL HCL ER, Tablet, 240 mg has the following code Pedigree: AD52778_94, EXP: 5/21/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 269 of 273

PRAMIPEXOLE DI-HCL, Tablet, 1.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68462033490

D-731-2014

Recall number: D-731-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 90 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; PRAMIPEXOLE DI-HCL, Tablet, 1.5 mg may be potentially mislabeled as LIOTHYRONINE SODIUM, Tablet, 25 mcg, NDC 42794001902, Pedigree: AD68010_11, EXP: 5/28/2014.

Code information

PRAMIPEXOLE DI-HCL, Tablet, 1.5 mg has the following code Pedigree: AD68010_20, EXP: 5/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 270 of 273

RASAGILINE MESYLATE, Tablet, 0.5 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 68546014256

D-732-2014

Recall number: D-732-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 30 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; RASAGILINE MESYLATE, Tablet, 0.5 mg may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 40985022921, Pedigree: W002690, EXP: 6/5/2014.

Code information

RASAGILINE MESYLATE, Tablet, 0.5 mg has the following code Pedigree: W002929, EXP: 6/10/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 271 of 273

MAGNESIUM CHLORIDE, Tablet, 64 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 68585000575

D-733-2014

Recall number: D-733-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 720 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MAGNESIUM CHLORIDE, Tablet, 64 mg may be potentially mislabeled as VITAMIN B COMPLEX W/C, Tablet, NDC 00904026013, Pedigree: AD52993_31, EXP: 5/17/2014; ASPIRIN EC, Tablet, 325 mg, NDC 00904201360, Pedigree: W003526, EXP: 6/21/2014; NICOTINE POLACRILEX, LOZENGE, 2 mg, NDC 00135051001, Pedigree: W002766, EXP: 6/6/2014; THIAMINE HCL, Tablet, 100 mg, NDC 00904054460, Pedig

Code information

MAGNESIUM CHLORIDE, Tablet, 64 mg has the following codes Pedigree: AD52993_4, EXP: 5/17/2014; Pedigree: W003527, EXP: 6/21/2014; Pedigree: W002712, EXP: 6/6/2014; Pedigree: W003359, EXP: 6/19/2014; Pedigree: W003923, EXP: 6/28/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 272 of 273

MELATONIN, Tablet, 1 mg, Over The Counter, Distributed by: AidaPak Service, LLC, NDC 74312002832

D-734-2014

Recall number: D-734-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 360 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; MELATONIN, Tablet, 1 mg may be potentially mislabeled as OMEGA-3 FATTY ACID, Capsule, 1000 mg, NDC 40985022921, Pedigree: W003711, EXP: 6/26/2014.

Code information

MELATONIN, Tablet, 1 mg has the following code Pedigree: W003717, EXP: 6/26/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

drug · product 273 of 273

HYOSCYAMINE SULFATE SL Tablet, 0.125 mg, Rx only, Distributed by: AidaPak Service, LLC, NDC 76439030910

D-735-2014

Recall number: D-735-2014
Initiated: July 02, 2013
Classification: Class II
Status: Terminated
Recalling firm: Aidapak Services, LLC
Quantity: 200 Tablets

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling:Label Mixup; HYOSCYAMINE SULFATE SL Tablet, 0.125 mg may be potentially mislabeled as azaTHIOprine, Tablet, 50 mg, NDC 00054408425, Pedigree: AD56832_1, EXP: 5/21/2014; CHOLECALCIFEROL, Tablet, 1000 units, NDC 00904582460, Pedigree: W003464, EXP: 6/20/2014.

Code information

HYOSCYAMINE SULFATE SL, Tablet, 0.125 mg has the following codes Pedigree: AD54501_1, EXP: 5/21/2014; Pedigree: W003438, EXP: 6/20/2014.

Distribution pattern

Repacked drugs were distributed in Arizona, California, Oregon, and Washington.

Event summary

Source snapshots represented here

Every recalled product in this event

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