Exact FDA event identifier

Event 77082

6 recalled-product records grouped only because every row carries this exact official event ID.

Event summary

Timeline bucket: April 20, 2017
Product types: Drug
Classifications: Class I and Class II
Statuses: Terminated
Recalling firm wording: C. O. Truxton

Dossier provenance

Source snapshots represented here

openFDA Drug Enforcement Report-date coverage June 20, 2012–July 08, 2026 Known gap: openFDA describes 2004-present coverage, but the current export has no report-date records in this interval.

Enforcement coverage uses report dates; product initiation dates can precede those bounds. Device-enrichment coverage uses FDA event_date_initiated.

How coverage and grouping work

Device root-cause evidence is not applicable to this event. No grouped product has the official product type device; this is not an unavailable-enrichment finding.

Complete imported group

Every recalled product in this event

6 official enforcement rows

Product dates, classifications, firms, and source wording remain attached to their individual rows. Opening this dossier never hides products that did not match a prior timeline filter.

drug · product 1 of 6

Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10

D-1111-2017

Recall number: D-1111-2017
Initiated: April 20, 2017
Classification: Class I
Status: Terminated
Recalling firm: C. O. Truxton
Quantity: unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

Labeling: Labeled Error

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Labeled Error on Declared Strength; report of a 1000 ct bottle labeled as Phenobarbital 15 mg tablets actually contained 30 mg tablets

Code information

Lot # 70952A; Exp. 11/17

Distribution pattern

Nationwide

drug · product 2 of 6

Phenobarbital Tablets USP, 30 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6145-10

D-1112-2017

Recall number: D-1112-2017
Initiated: April 20, 2017
Classification: Class I
Status: Terminated
Recalling firm: C. O. Truxton
Quantity: unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

mislabeled

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; potentially mislabeled

Code information

Lot # 70926A; Exp. 11/17 Lot # 70981A; Exp. 01/18 Lot # H15A59; Exp. 08/18

Distribution pattern

Nationwide

drug · product 3 of 6

Phenobarbital Tablets USP, 60 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6151-10

D-1113-2017

Recall number: D-1113-2017
Initiated: April 20, 2017
Classification: Class II
Status: Terminated
Recalling firm: C. O. Truxton
Quantity: unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

mislabeled

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; potentially mislabeled

Code information

Lot # 71416A; Exp. 05/20 Lot # 70881A; Exp. 07/17 Lot # H15A68; Exp. 01/18 Lot # 70980A; Exp. 02/18

Distribution pattern

Nationwide

drug · product 4 of 6

Phenobarbital Tablets USP, 100 mg, a) 100 count bottles (NDC 0463-6152-01), b) 1000 count bottles (NDC 0163-6152-10), Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031

D-1114-2017

Recall number: D-1114-2017
Initiated: April 20, 2017
Classification: Class II
Status: Terminated
Recalling firm: C. O. Truxton
Quantity: unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

mislabeled

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; potentially mislabeled

Code information

a) Lot # 70989A; Exp. 02/18, Lot # 70973A; Exp. 01/18 b) Lot # 70973A; Exp. 01/18, Lot # H15A76; Exp. 02/18, Lot # 71346A; Exp. 12/19, Lot # 70989A; Exp. 02/18

Distribution pattern

Nationwide

drug · product 5 of 6

Amitriptyline HCL Tablets, USP 50 mg, 100 count bottles, Rx Only, Manufactured for: Qualitest Pharmaceuticals Huntsville, AL 35811, Distributed by: Truxton, Inc. Bellmawr, NJ 08031, NDC: 0463-6352-10

D-1115-2017

Recall number: D-1115-2017
Initiated: April 20, 2017
Classification: Class II
Status: Terminated
Recalling firm: C. O. Truxton
Quantity: unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

mislabeled

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; potentially mislabeled

Code information

Lot # C0260416A; Exp. 03/18

Distribution pattern

Nationwide

drug · product 6 of 6

Phenobarbital Tablets USP, 15 mg, 1000 count bottles, Rx Only, Manufactured by West-ward Pharmaceutical Corp. Eatontown, NJ 07724, Distributed by Truxton, Inc., Bellmawr, NJ 08031, NDC 0463-6160-10

D-1116-2017

Recall number: D-1116-2017
Initiated: April 20, 2017
Classification: Class II
Status: Terminated
Recalling firm: C. O. Truxton
Quantity: unknown

App-derived interpretation

Labeling or packaging reason.labeling_packaging · v1.0.0

mislabeled

These labels are deterministic app interpretations, not FDA categories.

Inspect official wording and provenance

Reason for recall

Labeling: Label Mixup; potentially mislabeled

Code information

Lot # 71162A; Exp. 10/18 Lot # 70915A; Exp. 08/17 Lot # H15A55; Exp. 11/17

Distribution pattern

Nationwide