Bionpharma Inc. recalls Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc., P
Recalled July 29, 2026 · FDA recall D-0742-2026 · Bionpharma
Hazard
Presence of Foreign Tablets/Capsules · FDA Class II
Units
N/A
Sold at
US Nationwide.
Description
Presence of Foreign Tablets/Capsules
Product
Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc., Princeton, NJ 08540, Made in India, NDC 69452-435-30.
Manufacturer(s)
Bionpharma Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →