Bionpharma Inc.: Divalproex Sodium Delayed-release Tablets, Usp, 500 Mg, 500 Tablets Bottles
Recall Summary Bionpharma Inc. is recalling 500-tablet bottles of Divalproex Sodium Delayed-Release Tablets, USP, 500 mg (NDC 69452-435-30) distributed nationwide because some bottles contain foreign tablets or capsules mixed in with the correct medication. This recall affects patients in all U.S. states and territories who received this prescription drug.
- Recalling firm
- Bionpharma Inc.
- 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
- Presence of Foreign Tablets/Capsules
- Category
- drug recall
- Country
- United States
- Agency
- U.S. Food and Drug Administration
- Recall date
- 2026-06-26
- Status
- Ongoing
- Areas affected
- AL, AK, AZ, AR, CA, CO, CT, DE, FL, GA, HI, ID, ...
- Distribution
- US Nationwide.
Official recall notice from U.S. Food and Drug Administration
Recall details on Nibble Recalls: https://trynibble.app/recalls/072969db-7c2b-4217-b408-a83a01d1d0a2