FDAApril 14, 2025drug

Duloxetine Delayed-Release Capsules USP, 60 mg, 1000-count bottles, Rx Only, Manufactured by Towa Pharmaceutical Europe, S.L., Distributed by Breckenridge Pharmaceutical, Inc. Berkeley Heights, NJ 07922, NDC# 51991-748-10

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

The hazard

CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim 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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