FDAMarch 15, 2017drug

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

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

The hazard

Failed Dissolution Specifications; 9 month long term stability

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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