Treats cutaneous lesions. Sold as Panretin. Every FDA application for this active ingredient.
As of Nov 15, 2026, FDA lists 1 application for Alitretinoin (sold as Panretin), first approved Feb 2, 1999, with 0 new uses approved and 0 published complete response letters.
| Product | Part | Spending, 2025 | Change | Beneficiaries |
|---|---|---|---|---|
| Panretin | Part D | $1.1M | +7% | 77 |
| Approved | Application | Sponsor | Supplements | Marketing |
|---|---|---|---|---|
| Feb 2, 1999 | PanretinNDA 20886 · New molecular entity | Advanz Pharma | 4 | Marketed |
Applications, approvals and products come from FDA's Drugs@FDA data files, refreshed weekly, grouped by active ingredient as FDA spells it. Complete response letters are FDA's published letters. Medicare spending is CMS's Part D and Part B dashboard, matched to this ingredient by generic name; shortages are FDA's shortage list, matched by application number; clinical trials are ClinicalTrials.gov studies naming the ingredient as an intervention, refreshed daily; safety programs are FDA's REMS list, matched by application number or, for shared programs, by ingredient. Drugs@FDA
