Aurolife Pharma, LLC recalls Allergy (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 30-count bottles, Distributed by: Aurohealth LLC, 2572 Brunswi
Recalled September 25, 2019 · FDA recall D-1872-2019 · Aurolife Pharma
Hazard
Failed Impurities/Degradation Specifications · FDA Class II
Units
240 bottles
Sold at
Nationwide in the USA
Description
Failed Impurities/Degradation Specifications
Product
Allergy (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 30-count bottles, Distributed by: Aurohealth LLC, 2572 Brunswick Pike, Lawrenceville, NJ 08648; NDC 58602-820-09.
Manufacturer(s)
Aurolife Pharma, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →