Recall
FDAHealthDecember 6, 2024

Amerisource Health Services LLC — Duloxetine Delayed-Release Capsules USP, 60 mg, Rx only, 30 count bottles, Manufactured by: Aurobindo Pharma Limited, Hyderabad-500 090, India, For BluePoint Laborato

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
December 6, 2024

Nationwide in the USA

What's affected?

Product
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
Lot code
DT6023061B

Additional details

Lot DT6023061B Exp 01/31/2025

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 20,734 30-count bottles.

View original FDA notice →

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