US Drug Recall Register
Class III · Low risk Terminated Initiated Jan 7, 2013 (14 years ago)

Glycopyrrolate Tablets, USP, 1 mg, Rx Only, 100 tablets per bottle, Manufactured by…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Subpotent Drug

What was recalled

Glycopyrrolate Tablets, USP, 1 mg, Rx Only, 100 tablets per bottle, Manufactured by: West-ward Pharmaceutical Corp., Eatontown, NJ, 07724, NDC 0143-1250-01.

Recalling firm
West-ward Pharmaceutical Corp.
NDC code
0143-1250-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-164-2013

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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