Recall
FDAHealthMay 27, 2026

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.

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

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
May 27, 2026

Nationwide within the United States

What's affected?

Product
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.
Brand
NIACIN
UPC
0362175320469
Lot code
25282724A

Additional details

Lot #: 25282724A, Exp. Date 2027/01

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated Quantity affected: 3984 bottles.

View original FDA notice →

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