Class II Recall

Lupin Pharmaceuticals Inc.

Product
Rifampin Capsules USP, 300 mg, 30-count bottle; Rx Only, Manufactured for: Lupin Pharmaceuticals Baltimore, Maryland 21202, Manufactured by: Lupin Limited Aurangabad 431 210 India. NDC 68180-659-06
Reason
Failed Impurities/Degradation Specifications: Failure observed in related substance testing during long term stability study.
Classification
Class II
Status
Terminated
Lot
Lot # A200171, Exp 12/2023
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