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FDAApril 24, 2018drug

Amlodipine and Benazapril HCL Capsules, USP, 5 mg/40 mg, 100 count bottles, Mylan Pharmaceuticals, Inc., Morgantown, WV --- NDC 0378-6899-01

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

The hazard

cGMP Deviations; cleaning processes for equipment used to manufacture the specified batches was not followed according to procedure

What to do

FDA enforcement status: Terminated

Brands named

mylan pharmaceuticalsmylan

Recall history

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

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