FDA recall D-1873-2019

Aurolife Pharma, LLC · Class II · drug

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.

Reason for recall

Failed Impurities/Degradation Specifications

Distribution

Nationwide in the USA

Key facts

Status: Terminated
Initiation date: 2019-08-23
Report date: 2019-09-25
Termination date: 2022-08-16
Voluntary/Mandated: Voluntary: Firm initiated
Location: Dayton, NJ, United States

Primary source

https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-1873-2019