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.