Active ingredient
Deferiprone
10 finished FDA listings contain Deferiprone as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- DEFERIPRONE
- Dosage forms
- Solution, Tablet, Tablet, Coated, Tablet, Film Coated
- Routes
- Oral
- Manufacturers / labelers
- 5
- Strengths listed
- 100 mg/ml · 1000 mg/1 · 500 mg/1
- Brand names in FDA listings
- Ferriprox
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 11645
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 |
|---|---|---|---|
| NDA 021825 | CHIESI | 2011-10-14 | 1 |
| NDA 208030 | CHIESI | 2015-09-09 | 1 |
| ANDA 208800 | TARO | 2019-02-08 | 3 |
| NDA 212269 | CHIESI | 2020-05-19 | 1 |
| ANDA 213239 | HIKMA | 2021-03-29 | 2 |
| ANDA 220132 | SENORES PHARMS | 2025-12-11 | 2 |
Official labeling on DailyMed
- DEFERIPRONE TABLET [AVKARE] · version 1 · 2026-08-14
- FERRIPROX (DEFERIPRONE) TABLET FERRIPROX (DEFERIPRONE) TABLET, FILM COATED [CHIESI USA, INC.] · version 15 · 2026-01-30
- DEFERIPRONE TABLET, COATED [DR. REDDY'S LABORATORIES, INC.] · version 1 · 2025-12-16
- DEFERIPRONE TABLET, COATED [HIKMA PHARMACEUTICALS USA INC.] · version 3 · 2025-06-09
- DEFERIPRONE TABLET, COATED [HIKMA PHARMACEUTICALS USA INC.] · version 8 · 2025-06-09
- DEFERIPRONE TABLET [SUN PHARMACEUTICAL INDUSTRIES, INC.] · version 16 · 2025-05-30
- FERRIPROX (DEFERIPRONE) SOLUTION [CHIESI USA, INC.] · version 6 · 2025-05-26
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.