Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Penicillamine Tablets USP 250 mg Recalled by Lupin Pharmaceuticals Inc. Due to Failed Dissolution Specifications
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Lupin Pharmaceuticals Inc. directly.
Affected Products
Penicillamine Tablets USP 250 mg, 100-count bottle, Rx Only, Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 Manufactured by: Lupin Limited, Nagpur-441 108, India, NDC# 70748-153-01
Quantity: N/A
Why Was This Recalled?
Failed Dissolution Specifications
Where Was This Sold?
Product was distributed to 3 wholesale/distributor accounts.
About Lupin Pharmaceuticals Inc.
Lupin Pharmaceuticals Inc. has 119 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report