Drug recall D-0096-2026
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
Reason for recall
Failed Dissolution Specifications
Lots and codes
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
Recall details
- Recalling firm
- Lannett Company Inc., Seymour, IN
- Quantity
- 46,848 90-count bottles
- Distribution
- Nationwide in the USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- October 10, 2025
Related products
- Niacin – drug information
- NDC 62175-322 Niacin · Niacin 1000 mg/1 · Lannett Company, Inc.
- NDC 62175-320 Niacin · Niacin 500 mg/1 · Lannett Company, Inc.