US Drug Recall Register
Class II · Moderate risk Terminated Initiated Mar 2, 2023 (4 years ago)

Alprazolam Tablets, USP, 0.5mg, CIV, 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: Potential risk of Cross Contamination

What was recalled

Alprazolam Tablets, USP, 0.5mg, CIV, packaged in: a) 100-count bottle (NDC 51991-0705-01), b) 500-count bottle (NDC 51991-0705-05) and c) 1,000-count bottle (NDC 51991-0705-10), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.

Recalling firm
Breckenridge Pharmaceutical, Inc
NDC code
51991-0705-01
Origin
CT, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0459-2023

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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