US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 7, 2023 (4 years ago)

Glimepiride Tablets USP, 1 mg, Rx Only, Packaged in: a) 100-count bottle NDC…

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

Why it was recalled

CGMP Deviations: recalling drug products following an FDA inspection.

What was recalled

Glimepiride Tablets USP, 1 mg, Rx Only, Packaged in: a) 100-count bottle NDC 16729-001-01 UPC 3 16729 00101 4; b) 500-count bottle NDC 16729-001-16 UPC 3 16729 00116 8; Manufactured for: Accord Healthcare, Inc., Durham, NC 27703. Manufactured by: Intas Pharmaceuticals Limited, Pharmez, Ahmedabad-382 213, INDIA

Recalling firm
Accord Healthcare, Inc.
NDC code
16729-001-01
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0393-2023

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.

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