WhichRecall
Class IIReported 2025-06-11

Fluoxetine Tablets, USP, 20 mg, 28-count Carton (4x7 Unit-dose), Manufactured by: TORRENT PHARMACEUTIALS LTD., Indrad-382 721 INDIA; Manufactured for: TORRENT PHARMA INC., Basking Ridge, NJ 07920. NDC: 13668-473-91 (Carton); 13668-473-70 (Blister)

Recalled by Torrent Pharma Inc.

Reason for Recall

CGMP Deviations: Presence of N-Nitroso Fluoxetine exceeding interim acceptable intake limit.

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Recall Number
D-0456-2025
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-05-27
Reported
2025-06-11
Distribution
U.S. Nationwide.
Code Info
Lot# BDX6K001; Exp. Date: 06/30/2025
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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