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Amneal Pharmaceuticals of New York, LLC recalls Divalproex Sodium Extended-release Tablets, USP 250 mg, Rx Only, 100 tablets, Manufactured by: Amneal Pharmaceuticals Pv

Recalled April 3, 2024 · FDA recall D-0426-2024 · Amneal Pharmaceuticals of New York

Hazard
Failed dissolution specifications · FDA Class II
Units
21,452/100 count bottles
Sold at
Product was distributed nationwide.

Description

Failed dissolution specifications

Product
Divalproex Sodium Extended-release Tablets, USP 250 mg, Rx Only, 100 tablets, Manufactured by: Amneal Pharmaceuticals Pvt. Ltd. Ahmedabad, INDIA, Distributed by: Amneal Pharmaceuticals LLC, Bridgewater, NJ 08807, NDC 65162-755-10. NDC# 65162-755-10
Manufacturer(s)
Amneal Pharmaceuticals of New York, LLC

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov

Amneal Pharmaceuticals of New York, LLC recalls Divalproex Sodium Extended-release Tablets, USP 250 mg, Rx Only, 100 tablets, Manufactured by: Amneal Pharmaceuticals Pv | RecallWatchUSA