FDAJuly 19, 2017drug

Voriconazole Tablets, 200 mg, 20-count cartons (4 x 5) Unit Dose, Rx only, Manufactured for: AvKARE, Inc. Pulaski, TN 38478, NDC 50268-804-12

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

The hazard

Failed impurities/degradation specifications: Out of specification for a related compound C.

What to do

FDA enforcement status: Terminated

Brands named

avkare

Recall history

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

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