Lannett Company Inc.: 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 reason: Failed Dissolution Specifications: during 12M LT stability testing OOS low for Stage 3 dissolution at the 24-hour timepoint.. Recalled by Lannett Company Inc.. Distribution: Nationwide within the United States. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot #: 25282724A, Exp. Date 2027/01. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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