FDAFDA · Food and drugs·Recall number D-0742-2026
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.
Published July 29, 2026 · Recall initiated: June 26, 2026
Status when published: Ongoing — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Presence of Foreign Tablets/Capsules
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- DIVALPROEX SODIUM
- Manufacturer
- Bionpharma Inc.
- Distributor
- US Nationwide.
- Lot
- Lot# 704C003, Exp. 12/31/2028
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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