Active ingredient
Diflorasone
4 finished FDA listings contain Diflorasone as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- DIFLORASONE DIACETATE
- Dosage forms
- Cream, Ointment
- Routes
- Topical
- Manufacturers / labelers
- 2
- Strengths listed
- .5 mg/g · 5 mg/g
- Brand names in FDA listings
- Psorcon
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 91311
Drugs@FDA applications
Linked only where the FDA listing’s application number matches Drugs@FDA exactly. A listing in the NDC Directory does not by itself mean FDA approval.
| Application | Sponsor | Original approval | Listings |
|---|---|---|---|
| ANDA 075331 | SUN PHARMA CANADA | 1999-05-14 | 1 |
| ANDA 075508 | SUN PHARMA CANADA | 2000-04-24 | 2 |
| ANDA 207440 | RISING | 2017-02-27 | 1 |
Official labeling on DailyMed
- DIFLORASONE DIACETATE CREAM [SUN PHARMACEUTICAL INDUSTRIES, INC.] · version 7 · 2025-09-25
- DIFLORASONE DIACETATE OINTMENT [SUN PHARMACEUTICAL INDUSTRIES, INC.] · version 6 · 2025-07-07
- PSORCON (DIFLORASONE DIACETATE) CREAM [SUN PHARMACEUTICAL INDUSTRIES, INC.] · version 4 · 2025-07-04
- DIFLORASONE DIACETATE OINTMENT [RISING PHARMA HOLDINGS, INC.] · version 4 · 2023-06-26
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.