Akorn, Inc. recalls Betaxolol Ophthalmic Solution, USP 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL per bottle, Sterile, Rx Only, Manufactured by:
Recalled January 25, 2023 · FDA recall D-0135-2023 · Akorn
Hazard
CGMP Deviations: · FDA Class II
Units
6,273 bottles
Sold at
Nationwide in the USA
Description
CGMP Deviations:
Product
Betaxolol Ophthalmic Solution, USP 0.5%, (Betaxolol HCl 5.6 mg/mL), 5 mL per bottle, Sterile, Rx Only, Manufactured by: Akorn, Inc., Lake Forest, IL 60045. NDC: 17478-705-10
Manufacturer(s)
Akorn, Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →