Bionpharma Inc. recalls Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500
See all recalls from Bionpharma Inc. →Recalled 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.
Hazard / Issue
Presence of Foreign Tablets/Capsules
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot# 704C003, Exp. 12/31/2028
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Divalproex Sodium Delayed-Release Tablets, →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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