Lannett Company Inc. Recall: Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 T
Lannett Company Inc. Recall: Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 T is one of 9,000 recalls in the RecallGuard dataset. Key details — Recalling firm: Lannett Company Inc.; Product: Niacin Extended-release Tablets, USP, 1,000 mg, Rx Only, 90 Tablets per bottle, Distributed by: Lannett Company, Inc
| Recalling firm | Lannett Company Inc. |
|---|---|
| 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 |
| Classification | Class II (moderate — may cause temporary or reversible health consequences) |
| Status | Ongoing |
| Distribution | Nationwide in the USA |
| Recall initiated | 20251010 |
| Recall number | D-0096-2026 |
| Category | drug |
| State | IN |
| Country | United States |
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