FDAMay 27, 2026drug

Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 62175-322-46.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.

What to do

FDA enforcement status: Ongoing

Brands named

lannett

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distributed by: Lannett Company, Inc., Philadelphia, PA 19136, NDC 62175-322-46. — Recall Details · AllClear