Skip to content
Recall Observatory FDA recall evidence

Drug product

Indomethacin Capsules USP, 50 mg, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Colvale-Bardez, Goa 403513, India; Manufactured for: Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ 07430, NDC 68462-302-01.

D-0606-2018

March 19, 2018

Class III

Product summary

Firm
Glenmark Pharmaceuticals Inc., USA
Event
Event 79570
Status
Terminated
Classification
Class III
Quantity
109,080 Bottles
Official record key
drug-enforcement:D-0606-2018

Official wording

Reason: Labeling: Incorrect Instructions: bottles incorrectly labeled with the usual adult dosage of "One or two capsules 2 or 3 times a day." rather than the correct usual adult dosage of "One capsule 2 or 3 times a day.

Code information: Lot #: 19172776, 19172794, Exp 07/19; 19173111, 19173186, 19173188, 19173189, Exp 08/19; 19173852, 19173878, 19173893, Exp 10/19; 19174318, 19174341, Exp 11/19.

Distribution pattern: Nationwide in the United States.

Derived failure modes

  • Labeling or packaging

    reason.labeling_packaging · v1.0.0

    Labeling: Incorrect