Sold as Florone, Psorcon E, Florone E, Psorcon. Every FDA application for this active ingredient: 5 branded and 8 generic.
As of Nov 15, 2026, FDA lists 13 applications for Diflorasone Diacetate (sold as Florone, Psorcon E, Florone E and others), first approved Sep 14, 1977, with 0 new uses approved and 0 published complete response letters.
| Product | Part | Spending, 2025 | Change | Beneficiaries |
|---|---|---|---|---|
| Diflorasone Diacetate | Part D | $15.4M | -17% | 7,478 |
| Sep 14, 1977 | FloroneNDA 17741 · New molecular entity | Pfizer | 20 | Discontinued |
| Mar 1, 1978 | Psorcon ENDA 17994 · New dosage form | Pfizer | 22 | Discontinued |
| Aug 28, 1985 | Florone ENDA 19259 · New dosage form | Pfizer | 9 | Discontinued |
| Aug 28, 1985 | PsorconNDA 19260 · New dosage form | Pfizer | 7 | Discontinued |
| Nov 20, 1992 | PsorconNDA 20205 · New formulation or manufacturer | Taro Pharms North | 2 | Discontinued |
| Mar 30, 1998 | Diflorasone DiacetateANDA 75187 | Avondale Pharms | 3 | Discontinued |
| Apr 27, 1999 | Diflorasone DiacetateANDA 75374 | Avondale Pharms | 5 | Marketed |
| May 14, 1999 | Diflorasone DiacetateANDA 75331 | Sun Pharma Canada | 3 | Marketed |
| Apr 24, 2000 | Diflorasone DiacetateANDA 75508 | Sun Pharma Canada | 4 | Marketed |
| Dec 20, 2002 | Diflorasone DiacetateANDA 76263 | Ani Pharms | 3 | Discontinued |
| Jul 24, 2015 | Diflorasone DiacetateANDA 206572 | Sciegen Pharms | 0 | Discontinued |
| Feb 27, 2017 | Diflorasone DiacetateANDA 207440 | Rising | 0 | Marketed |
| Jun 12, 2018 | Diflorasone DiacetateANDA 210753 | The J Molner | 0 | 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