US Drug Recall Register
Class II · Moderate risk Completed Initiated Dec 22, 2022 (4 years ago)

Glycopyrrolate Tablets, USP, 1 mg, 50 Tablets (5x10) Unit Dose carton, Rx Only…

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

Failed impurities/degradation specifications: Out of specification for unknown impurities.

What was recalled

Glycopyrrolate Tablets, USP, 1 mg, 50 Tablets (5x10) Unit Dose carton, Rx Only, Manufactured for: AvKARE Pulaski, TN 38478, NDC 50268-363-15

Recalling firm
Avkare LLC
NDC code
50268-363-15
Origin
TN, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0091-2023

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.

Other Glycopyrrolate recalls

See all