FDAOctober 6, 2017drug

Duloxetine Delayed-release Capsules USP, 20 mg, 50 Capsules (5 x 10) Unit Dose per carton, unit dose blister UPC 5026828311), Rx only, Manufactured for: AvKARE, Inc., Pulaski, TN 38478, NDC 50268-283-15.

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

The hazard

Failed Impurities/Degradation Specifications: slightly elevated levels of phthalic acid.

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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