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Class II · ModerateActive recall

Divalproex Sodium

Could cause temporary or reversible harm; serious harm is unlikely.

Does this affect you?
Check your lot numberLot# 704C003, Exp. 12/31/2028
Where it was soldUS Nationwide.
Find the lot number printed on your box or bottle. If it matches — and you take this medicine — call your pharmacist. Don't stop a prescribed medicine on your own.

What happened

Presence of Foreign Tablets/Capsules

What to do

  1. Check the lot number and expiry on your medicine against the recall above.
  2. Talk to your pharmacist or doctor before changing anything — don't stop on your own.
  3. Report any problems to FDA MedWatch (1-800-FDA-1088 or fda.gov/medwatch).

Who makes it

Made byMade in India foreign manufacturer
Brand nameDIVALPROEX SODIUM
Generic nameDIVALPROEX SODIUM
Active ingredient(s)DIVALPROEX SODIUM
Distributed by / forBionpharma Inc., Princeton, NJ 08540
NDC69452-435-30
Show the full FDA record
Full product labelDivalproex 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.
Recalling firmBionpharma Inc.
DistributionUS Nationwide.
QuantityN/A
Recall initiated2026-06-26
Report date2026-07-29
Recall completed—
Recall numberD-0742-2026
ClassificationClass II
FDA statusOngoing
Origin on filePrinceton NJ United States

Related

Recent drug recallsCheck another medication

Source: U.S. FDA enforcement database (openFDA). Look this up on the official FDA recalls site ↗

This is public FDA recall information, not medical advice. A recall does not always mean your specific bottle is affected. Never stop a prescribed medicine without asking your pharmacist or doctor.