FDAJanuary 13, 2025drug

Duloxetine Delayed-Release Capsules USP, 20 mg, packaged in a) 30 Unit Doses (3x10 blister packs) NDC 0904-7043-04 and b) 100 Unit Doses (10x10 blister packs) NDC 0904-7043-61, Rx only, Packaged and Distributed by: Major Pharmaceuticals, Indianapolis, IN 46268 USA.

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

The hazard

CGMP Deviations: presence of Nitrosamine Drug Substances Related Impurity (NDSRI), N-Nitroso-Duloxetine above the FDA recommended acceptable intake limit

What to do

FDA enforcement status: Terminated

Brands named

harvard drug group llc dba major pharmaceuticals and rugby laboratoriesharvardharvard drug

Recall history

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

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