Reported Jul 29, 2026 · Ongoing

Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only, Distributed by: Bionpharma Inc.,…

Bionpharma Inc.

Moderate riskThis product could cause temporary or reversible health problems — stop using it.

What you should do

Stop using the affected lot and contact the recalling firm for the return or refund process. Check the FDA enforcement report for lot-level detail.

Firm contact: Bionpharma Inc. · 400 Alexander Park Ste 2-4b · Princeton, NJ · 08540-6539

Is this the product you have?

  • Divalproex Sodium Delayed-Release Tablets, USP, 500 mg, 500 Tablets bottles, Rx only
  • Distributed byBionpharma Inc., Princeton, NJ 08540, Made in India, NDC 69452-435-30
Lot codes and dates
    • Lot# 704C003
    • Exp. 12/31/2028
Amount recalled
N/A

Where it was sold

  • Nationwide

Why it was recalled

Presence of Foreign Tablets/Capsules

This product could cause temporary or reversible health problems — stop using it.

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Where this came from

Source: U.S. Food & Drug Administration (openFDA)

Read the FDA (openFDA drug enforcement) notice

Data as of Sep 19, 3:29 PM UTC

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