Recall
FDAHealthJune 26, 2026

Bionpharma Inc. — 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.

⚠️ Presence of Foreign Tablets/Capsules

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
June 26, 2026

US Nationwide.

What's affected?

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.
Lot code
704C003

Additional details

Lot# 704C003, Exp. 12/31/2028

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: N/A.

View original FDA notice →

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