US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 9, 2013 (13 years ago)

Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY…

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

Why it was recalled

Failed Tablet/Capsule Specifications; partial tablet erosion resulting in tablet weights below specification in some tablets

What was recalled

Alprazolam Orally Disintegrating Tablets, USP 2 mg, 100 count bottles, Rx Only, MFG. BY ACTAVIS ELIZABETH LLC., Elizabeth, NJ, NDC 0228-4025-11

Recalling firm
Actavis Elizabeth LLC
NDC code
0228-4025-11
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-018-2014

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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