Sold as Cyclocort. Every FDA application for this active ingredient: 3 branded and 5 generic.
As of Nov 14, 2026, FDA lists 8 applications for Amcinonide (sold as Cyclocort), first approved Oct 18, 1979, with 0 new uses approved and 0 published complete response letters.
| Product | Part | Spending, 2025 | Change | Beneficiaries |
|---|---|---|---|---|
| Amcinonide | Part D | $11.7M | +162% | 1,995 |
| Oct 18, 1979 | CyclocortNDA 18116 · New molecular entity | Astellas | 9 | Discontinued |
| Nov 13, 1981 | CyclocortNDA 18498 · New dosage form | Astellas | 11 | Discontinued |
| Jun 13, 1988 | CyclocortNDA 19729 · New dosage form | Astellas | 7 | Discontinued |
| May 31, 2002 | AmcinonideANDA 76229 | Taro Pharm Inds | 0 | Marketed |
| Nov 6, 2002 | AmcinonideANDA 76329 | Solubiomix | 0 | Marketed |
| Nov 19, 2002 | AmcinonideANDA 76096 | Genus | 0 | Marketed |
| Mar 19, 2003 | AmcinonideANDA 76367 | Taro Pharm Inds | 0 | Discontinued |
| May 15, 2003 | AmcinonideANDA 76065 | Genus Lifesciences | 0 | Discontinued |
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