Lannett Company, Inc. Recalls

1 recall found for Lannett Company, Inc.. Check if any of your products are affected.

HIGHFDA DRUG

Lannett Company Recalls Niacin Tablets for Failed Dissolution

Lannett Company, Inc. recalled 46,848 bottles of Niacin Extended-release Tablets on October 10, 2025. The recall follows reports of failed dissolution specifications, which could affect medication effectiveness. Consumers should stop using the product immediately and consult healthcare providers for guidance.

NIACIN
Failed Dissolution
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Brand Statistics

Total Recalls
1
Pages
1

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