Bionpharma recalls Divalproex Sodium 500 mg delayed-release tablets over foreign tablets or capsules found in bottles
The notice says the 500-tablet bottles of Divalproex Sodium Delayed-Release Tablets, 500 mg, may contain foreign tablets or capsules, meaning pills that do not belong in the bottle.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- 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.
- Company
- Bionpharma Inc.
- Hazard
- Presence of Foreign Tablets/Capsules
- Units
- N/A
- Where sold
- US Nationwide.
- FDA classification
- Class II · Ongoing
- Classified by FDA
- August 6, 2026
- Recall started
- June 26, 2026
- FDA enforcement report
- July 29, 2026
- Identifiers
- Codes: Lot# 704C003, Exp. 12/31/2028
- FDA recall number: D-0742-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- 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
- Classification
- Class II (Ongoing)
- Distribution
- US Nationwide.
- Quantity
- N/A
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