Drug recall D-0742-2026
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.
Reason for recall
Presence of Foreign Tablets/Capsules
Lots and codes
Lot# 704C003, Exp. 12/31/2028
Recall details
- Recalling firm
- Bionpharma Inc., Princeton, NJ
- Quantity
- N/A
- Distribution
- US Nationwide.
- Type
- Voluntary: Firm initiated
- Recall initiated
- June 26, 2026
Related products
- Divalproex Sodium – drug information
- NDC 69452-435 divalproex sodium · Divalproex Sodium 500 mg/1 · Bionpharma Inc.
- NDC 69452-433 divalproex sodium · Divalproex Sodium 125 mg/1 · Bionpharma Inc.
- NDC 69452-434 divalproex sodium · Divalproex Sodium 250 mg/1 · Bionpharma Inc.