FDAApril 21, 2026drug

Duloxetine Delayed-Release Capsules USP, 60mg, Rx Only, 90-count bottle, Mfr. by Towa Pharmaceutical Eurpoe S.L., Martorelles, (Barcelona), Spain, Dist. by. Breckenridge Pharmaceutical, Inc., Berkely Heights, NJ 07922, NDC 51991-748-90.

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

The hazard

CGMP Deviations; presence of N-nitroso-duloxetine impurity above the FDA recommended limit

What to do

FDA enforcement status: Ongoing

Brands named

breckenridge pharmaceuticalbreckenridge

Recall history

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

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