company
Lannett Company Inc.
Jurisdiction: US
FDA Warning Letter timeline
V1 scope: FDA Warning Letters only. Additional public-record sources (SEC, CPSC, federal contracts) are on the V2 roadmap and are not surfaced here today.
- fda_recall · drug_recall2026-06-10Lannett Company Inc. — Class II recall: Niacin Extended-release Tablets, USP, 1,000 mg, 90-count bottles, Rx Only, Distr…
- fda_recall · drug_recall2026-05-27Lannett Company Inc. — Class III recall: Primidone Tablets USP, 250mg, 100-count bottle, Rx only, Distributed by: Lannett…
Frequently asked questions
- How many FDA warning letters has Lannett Company Inc. received?
- Argus HQ has not recorded an FDA warning letter for Lannett Company Inc. in our current dataset.
- What FDA recalls has Lannett Company Inc. issued?
- Argus HQ has recorded 2 FDA recalls tied to Lannett Company Inc..
- Is Lannett Company Inc. FDA compliant?
- Argus HQ is not a compliance rating service. As of this page's last update, our dataset shows 0 warning letters, 2 recalls, and 0 approval records for Lannett Company Inc.. Review the linked FDA source records directly before drawing a compliance conclusion.
Informational only. FDA Warning Letters are public records (17 USC §105). Summaries are AI-assisted and may contain errors; always verify against the original FDA letter before acting. Not legal, financial, or regulatory advice.

