Active ingredient
Alclometasone
3 finished FDA listings contain Alclometasone as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- ALCLOMETASONE DIPROPIONATE
- Dosage forms
- Cream, Ointment
- Routes
- Topical
- Manufacturers / labelers
- 2
- Strengths listed
- .5 mg/g
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 108088
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 076730 | SUN PHARMA CANADA | 2004-07-29 | 1 |
| ANDA 076587 | SUN PHARMA CANADA | 2005-09-15 | 1 |
| ANDA 079227 | GLENMARK PHARMS LTD | 2009-07-30 | 1 |
Official labeling on DailyMed
- ALCLOMETASONE DIPROPIONATE OINTMENT [SUN PHARMACEUTICAL INDUSTRIES, INC.] · version 6 · 2025-08-15
- ALCLOMETASONE DIPROPIONATE CREAM [SUN PHARMACEUTICAL INDUSTRIES, INC.] · version 8 · 2025-07-31
- ALCLOMETASONE DIPROPIONATE CREAM ALCLOMETASONE DIPROPIONATE OINTMENT [GLENMARK PHARMACEUTICALS INC., USA] · version 15 · 2024-01-18
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.