Fexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 30-count carton (NDC 70677-0008-2) and b) 15-count carton (NDC 70677-0008-1), sunmark, Distributed by McKesson, One Post Street, San Francisco, CA 94104.
Recall Number: D-1868-2019
Firm: Aurolife Pharma, LLC
Classification: Class II
Status: Terminated
Report Date: 20190925
Initiation Date: 20190823
Termination Date: 20220816
Reason for Recall
Failed Impurities/Degradation Specifications
Product Description
Fexofenadine Hydrochloride Tablets USP, 180 mg, packaged in a) 30-count carton (NDC 70677-0008-2) and b) 15-count carton (NDC 70677-0008-1), sunmark, Distributed by McKesson, One Post Street, San Francisco, CA 94104.