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
Reported: October 29, 2025 Initiated: October 10, 2025 #D-0096-2026
Product Description
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
Details
- Recalling Firm
- Lannett Company Inc.
- Units Affected
- 46,848 90-count bottles
- Distribution
- Nationwide in the USA
- Location
- Seymour, IN
Frequently Asked Questions
What product was recalled? ▼
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.. Units affected: 46,848 90-count bottles.
Why was this product recalled? ▼
Failed Dissolution Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on October 29, 2025. Severity: Moderate. Recall number: D-0096-2026.
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