United StatesDivalproex Sodium Delayed‑Release Tablets, USP 500 mg, 500‑count prescription bottles (NDC 69452‑435‑30), distributed by Bionpharma Inc., Princeton, NJ, made in India, Lot 704C003, exp. 12/31/2028, are being recalled. The recall is due to the presence of foreign tablets or capsules found in the product.
What's being recalled
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.
Recalling firm: Bionpharma Inc., Princeton, NJ, United States.
How to identify it
Lot# 704C003, Exp. 12/31/2028
The hazard
Presence of Foreign Tablets/Capsules
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)