WhichRecall
Class IIReported 2025-10-29

Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136. NDC: 62175-322-46

Recalled by Lannett Company Inc.

Reason for Recall

Failed Dissolution Specifications

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Recall Number
D-0096-2026
Classification
Class II
Status
Ongoing
Category
drug
Initiated
2025-10-10
Reported
2025-10-29
Distribution
Nationwide in the USA
Code Info
Lot, expiry: 21264027A, Exp 10/30/2025; 22266446A, Exp 12/31/2025; 22266901A, Exp 02/28/2026; 22267553A, 22267554A, Exp 03/31/2026; 22267555A, Exp 02/28/2026; 22267992A, Exp 04/30/2026; 22267993A, 22267994A, Exp 05/31/2026
Source: openFDA enforcement report. WhichRecall is not affiliated with the FDA. See our disclaimer.
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