Class II

Drug Recall: 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

Lannett Company Inc. · October 10, 2025

Reason for Recall

Failed Dissolution Specifications

Distribution

Nationwide in the USA

States Affected

NATIONWIDE

Quantity Affected

46,848 90-count bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0096-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.

Lannett Company Inc. Drug Recall: 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 | SafeCheck