US Drug Recall Register
Class II · Moderate risk Terminated Initiated Jan 31, 2019 (8 years ago)

Divalproex Sodium Extended-release Tablets, USP 250 mg, 100-count bottle, Rx only…

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

Why it was recalled

Failed Dissolution Specifications: Out of specification results observed for high dissolution.

What was recalled

Divalproex Sodium Extended-release Tablets, USP 250 mg, 100-count bottle, Rx only, Mfd.By: Dr. Reddy's Laboratories Limited Bachupally - 500 090 India NDC 55111-533-01

Recalling firm
Dr. Reddy's Laboratories, Inc.
NDC code
55111-533-01
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0507-2019

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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