FDAMay 10, 2017drug

Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-033-01) b.) 500-count bottle (NDC 68382-033-05), Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Dissolution Specifications

What to do

FDA enforcement status: Terminated

Brands named

zydus pharmaceuticalszydus

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-033-01) b.) 500-count bottle (NDC 68382-033-05), Rx only, manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distributed by: Zydus Pharmaceuticals, Pennington, NJ 07054 — Recall Details · AllClear