US Drug Recall Register
Class II · Moderate risk Terminated Initiated Feb 4, 2014 (13 years ago)

Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only…

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

Why it was recalled

Failed Dissolution Specifications: Product did not meet specification requirements for dissolution.

What was recalled

Alprazolam Extended-Release Tablets, USP, 3 mg, 60-count tablets per bottle, Rx only, Manufactured by: Actavis Elizabeth LLC, 200 Elmora Avenue, Elizabeth, NJ 07207, NDC 0228-3086-06, UPC 3 0228-3086-06 2.

Recalling firm
Actavis Elizabeth LLC
NDC code
0228-3086-06
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1091-2014

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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