Why it was recalled
Presence of Foreign Tablets/Capsules
Product description
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.
Lot numbers, UPCs & expiration codes
Lot# 704C003, Exp. 12/31/2028
Where it was sold
US Nationwide.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0742-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Jun 26, 2026
- FDA report date
- Jul 29, 2026
- Quantity
- N/A
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Bionpharma Inc.
Original FDA data
Every field from FDA enforcement report D-0742-2026, exactly as published.
Show all FDA fields
- City
- Princeton
- State
- NJ
- Status
- Ongoing
- Country
- United States
- Event ID
- 99316
- Address
- 400 Alexander Park Ste 2-4b
- Code information
- Lot# 704C003, Exp. 12/31/2028
- Postal code
- 08540-6539
- Report date
- Jul 29, 2026
- Product type
- Drugs
- Recall number
- D-0742-2026
- Classification
- Class II
- Recalling firm
- Bionpharma Inc.
- Reason for recall
- Presence of Foreign Tablets/Capsules
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- 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.
- Distribution pattern
- US Nationwide.
- Recall initiation date
- Jun 26, 2026
- Initial firm notification
- Letter
- Center classification date
- Aug 6, 2026