FDAOctober 21, 2015drug

Duloxetine Delayed-release Capsules, USP, 60 mg, Rx Only, 1000 count bottle, Manufactured by: Laboratorios Dr. Esteve, S.A., Barcelona, Spain, Distributed by: Breckenridge Pharmaceutical, Inc., Boca Raton, FL 33487, NDC: 51991-748-10

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

The hazard

Presence of Foreign Tablets/Capsules: one foreign capsule identified as omeprazole 10 mg was found in the bottle

What to do

FDA enforcement status: Terminated

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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