United States · FDA National Drug Code directory
FeraBright
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 24338-510_ac5e7507-8e66-4da5-abd9-75ae80369b9f
- Product NDC
- 24338-510
- Form
- INJECTION
- Composition / generic term
- Ferumoxytol
- Labeler
- Azurity Pharmaceuticals, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20251020
- Source listing expiry
- 20261231
Source-listed ingredients
- FERUMOXYTOL — 30 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-DOSE in 1 CARTON (24338-510-17) / 17 mL in 1 VIAL, SINGLE-DOSE · 24338-510-17
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →