MedicineWatch US
Class II Recall

SUN PHARMACEUTICAL INDUSTRIES INC

Product
Buprenorphine Sublingual Tablets, 8 mg, 30 count-bottles, Rx only, Manufactured by: Sun Pharma, NDC 62756-460-83.
Reason
CGMP Deviations
Classification
Class II
Status
Terminated
Lot
Lot #: DND1515A, Exp 08/24
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.