Lannett Company Inc. recalls Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle, Distributed by: Lannett Company, Inc., P
Recalled October 29, 2025 · FDA recall D-0096-2026 · Lannett
Hazard
Failed Dissolution Specifications · FDA Class II
Units
46,848 90-count bottles
Sold at
Nationwide in the USA
Description
Failed Dissolution Specifications
Product
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
Manufacturer(s)
Lannett Company Inc.
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →