Active ingredient
Amcinonide
4 finished FDA listings contain Amcinonide as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- AMCINONIDE
- Dosage forms
- Cream, Ointment
- Routes
- Topical
- Manufacturers / labelers
- 4
- Strengths listed
- 1 mg/g
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 17652
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 076229 | TARO PHARM INDS | 2002-05-31 | 1 |
| ANDA 076096 | GENUS | 2002-11-19 | 1 |
| ANDA 076367 | TARO PHARM INDS | 2003-03-19 | 1 |
| ANDA 076065 | GENUS LIFESCIENCES | 2003-05-15 | 1 |
Official labeling on DailyMed
- AMCINONIDE OINTMENT [AYURAX, LLC] · version 3 · 2025-11-17
- AMCINONIDE CREAM [INA PHARMACEUTICS INC.] · version 3 · 2025-07-08
- AMCINONIDE CREAM AMCINONIDE OINTMENT [SUN PHARMACEUTICAL INDUSTRIES, INC.] · version 5 · 2025-04-07
- AMCINONIDE CREAM [FOUGERA PHARMACEUTICALS INC.] · version 8 · 2022-07-04
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.