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FDAAugust 23, 2019drug

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.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Impurities/Degradation Specifications

What to do

FDA enforcement status: Terminated

Brands named

aurolife pharmaaurolife

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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