Aurolife Pharma, LLC recalls Wal-Fex (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 5-count cartons, Distributed By: Walgreen Co., 200 Wilmot Rd.,
Recalled September 25, 2019 · FDA recall D-1873-2019 · Aurolife Pharma
Hazard
Failed Impurities/Degradation Specifications · FDA Class II
Units
4920 cartons
Sold at
Nationwide in the USA
Description
Failed Impurities/Degradation Specifications
Product
Wal-Fex (Fexofenadine Hydrochloride) Tablets USP, 180 mg, 5-count cartons, Distributed By: Walgreen Co., 200 Wilmot Rd., Deerfield, IL 60015, NDC 0363-0097-55.
Manufacturer(s)
Aurolife Pharma, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →