Class III Recall

Akorn, Inc.

Product
Oxycodone Hydrochloride Oral Solution, USP 5 mg per 5 mL (1 mg/mL), 500 mL bottle, Rx only, Manufactured by: Hi-Tech Pharmacal Co., Inc., Amityville, NY 11701 --- NDC 50383-961-34
Reason
Labeling: Missing Label
Classification
Class III
Status
Terminated
Lot
Lots: 377186 Exp. 2/28/2023; 377188 Exp. 3/31/2023
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.
Akorn, Inc. — Class III Recall | MedicineWatch US