US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 11, 2012 (14 years ago)

Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for…

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

Why it was recalled

Tablet Separation: Possibility of cracked or split coating on the tablets.

What was recalled

Perphenazine Tablets, USP, 8 mg, 100-count tablets per bottle, Manufactured for: Qualitest Pharmaceuticals, Huntsville, AL 35811, NDC 0603-5092-21.

Recalling firm
Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals
NDC code
0603-5092-21
Origin
AL, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-010-2013

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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