FDADecember 2, 2024drug

Duloxetine Delayed-Release Capsules, 60 mg, a) 30 count blister cards (NDC 70518-0937-04), b) 30 count bottles (NDC 70518-0937-03), Rx only, Source NDC 57237-0019-99, MFG: Rising Pharma, Inc., Allendale, NJ, Repackaged by: RemedyRepack Inc., Indiana, PA

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

The hazard

CGMP Deviations; presence of N-nitroso-duloxetine impurity above recommended interim limit.

What to do

FDA enforcement status: Ongoing

Brands named

remedyrepack

UPCs

705180937047051809370357237001999

Recall history

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

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