Active ingredient
Ferumoxytol
4 finished FDA listings contain Ferumoxytol as their only active ingredient.
FDA NDC Directory
- Ingredient names as written by FDA
- FERUMOXYTOL, FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE
- Dosage forms
- Injection
- Routes
- Intravenous
- Manufacturers / labelers
- 3
- Strengths listed
- 30 mg/ml · 510 mg/17ml
- Brand names in FDA listings
- Ferabright, Feraheme
RxNorm (National Library of Medicine)
Ingredient concept RxCUI 473387
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 022180 | AZURITY | 2009-06-30 | 1 |
| ANDA 206604 | SANDOZ | 2021-01-15 | 1 |
| NDA 219868 | AZURITY | 2025-10-16 | 2 |
Official labeling on DailyMed
- FERUMOXYTOL INJECTION [SANDOZ INC] · version 7 · 2026-08-17
- FERAHEME (FERUMOXYTOL) INJECTION [AMAG PHARMACEUTICALS, INC] · version 23 · 2026-06-04
- FERABRIGHT (FERUMOXYTOL) INJECTION [AZURITY PHARMACEUTICALS, INC.] · version 2 · 2025-11-17
Sources: FDA NDC Directory (2026-09-29), RxNorm, Drugs@FDA, DailyMed. Each source’s facts are shown separately as published.