MedicineWatch US
Class II Recall

Direct Rx

Product
Finasteride, USP, 5 mg Tablets, Rx Only, Packaged as a 90-count bottle, NDC 61919-0733-90; Packaged and Distributed By: Direct Rx
Reason
cGMP deviations
Classification
Class II
Status
Terminated
Lot
Lot, expiry: 19AU2205, exp 12/31/24; 12OC2211, exp 12/31/24
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.
Direct Rx — Class II Recall | MedicineWatch US