NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals, Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274. Packaged by GSMS, Incorporated, Carmarillo, CA 93012. NDC: 51407-268-90
Reported: November 26, 2025 Initiated: October 20, 2025 #D-0158-2026
Product Description
NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals, Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274. Packaged by GSMS, Incorporated, Carmarillo, CA 93012. NDC: 51407-268-90
Reason for Recall
Failed Dissolution Specifications
Details
- Recalling Firm
- Golden State Medical Supply Inc.
- Units Affected
- 24,869 bottles
- Distribution
- Nationwide in the USA
- Location
- Camarillo, CA
Frequently Asked Questions
What product was recalled? ▼
NIACIN Extended-Release Tablets, USP, 1,000 mg, 90 tablets per bottle, Rx only, Manufactured by: Kremers Urban Pharmaceuticals, Inc., a subsidiary of Lannett Company, Inc., Seymour, IN 47274. Packaged by GSMS, Incorporated, Carmarillo, CA 93012. NDC: 51407-268-90. Recalled by Golden State Medical Supply Inc.. Units affected: 24,869 bottles.
Why was this product recalled? ▼
Failed Dissolution Specifications
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on November 26, 2025. Severity: Moderate. Recall number: D-0158-2026.
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