Recalls / Active ingredient / Divalproex Sodium

Divalproex Sodium

8 FDA drug recalls involving the active ingredient “Divalproex Sodium”.

Date	Class	Product	Firm
2023-12-26	Class II	Divalproex Sodium Extended-release Tablets, USP 250 mg, Rx Only, 100 tablets, Manufactured by: Amneal Pharmace	Amneal Pharmaceuticals of New York, LLC
2022-07-27	Class II	Divalproex Sodium Extended Release Tablets, USP, 250 mg, packaged in 100-count bottle, Rx only, Manufactured b	Amneal Pharmaceuticals of New York, LLC
2022-06-27	Class II	Divalproex Sodium Delayed-Release Tablets, USP 500mg, Rx Only, 100 Tablets, Distributed by: Sun Pharmaceutical	SUN PHARMACEUTICAL INDUSTRIES INC
2019-04-24	Class II	DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS, USP Tablets, 250 mg, 100 count-unit dose carton, RX only, Manufact	MAJOR PHARMACEUTICALS
2019-01-31	Class II	Divalproex Sodium Extended-release Tablets, USP 250 mg, 100-count bottle, Rx only, Mfd.By: Dr. Reddy's Laborat	Dr. Reddy's Laboratories, Inc.
2017-12-19	Class II	Divalproex Sodium Delayed Release Tablets USP, 500 mg, 100-count bottle, RX Only, Manufactured by: Unichem Lab	Unichem Pharmaceuticals Usa Inc
2015-05-22	Class II	Divalproex Sodium Extended-Release Tablets, USP, (valproic acid activity), 250 mg, 100 count (NDC 55111-533-01	Dr. Reddy's Laboratories, Inc.
2015-05-22	Class II	Divalproex Sodium Extended-Release Tablets, USP, 500 mg, 100 count bottles, Rx Only, Mfd. By. Dr. Reddy's Lab	Dr. Reddy's Laboratories, Inc.