MedicineWatch US
Class II Recall

Lupin Pharmaceuticals Inc.

Product
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
Reason
Failed Dissolution Specifications
Classification
Class II
Status
Terminated
Lot
Lot # M200498, Exp. June 2024
Date
Disclaimer: This tool indexes published US FDA drug-enforcement recall records from all countries, limited to the latest five years. A company or product not appearing here is not proof that it is compliant, approved, safe, or free of FDA action.
Lupin Pharmaceuticals Inc. — Class II Recall | MedicineWatch US