WhichRecall
Class IIReported 2025-01-01

Duloxetine Delayed-Release Capsules USP, 60 mg, Rx only, 30 count bottles, Manufactured by: Aurobindo Pharma Limited, Hyderabad-500 090, India, For BluePoint Laboratories NDC 68001-415-04

Recalled by Amerisource Health Services LLC

Reason for Recall

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above the recommended interim limit.

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Recall Number
D-0157-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2024-12-06
Reported
2025-01-01
Distribution
Nationwide in the USA
Code Info
Lot DT6023061B Exp 01/31/2025
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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