WhichRecall
Class IIReported 2025-04-09

Duloxetine Delayed-Release Capsules, USP, 30 mg, Rx Only, 1,000 Capsules per bottle, Manufactured by: Towa Pharmaceutical Europe, S.L., Martorelles, (Barcelona), Spain, Distributed by: Breckenridge Pharmaceutical, Inc., Berkley Heights, NJ 07922, NDC 51991-747-10.

Recalled by Breckenridge Pharmaceutical, Inc.

Reason for Recall

CGMP Deviations: presence of Nitrosamine Drug Substance Related Impurity (NDSRI), N-nitroso-duloxetine, above the recommended interim limit.

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Recall Number
D-0308-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-03-26
Reported
2025-04-09
Distribution
Nationwide in the US
Code Info
Lot 240909C, Exp Date 03/31/2027
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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