Prescription drug · NDA
FeraBright (Ferumoxytol) NDC 24338-310
Ferumoxytol 30 mg/mL · Injection · Intravenous · Azurity Pharmaceuticals, Inc.
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 24338-310-10 | 24338031010 | 1 VIAL, SINGLE-DOSE in 1 CARTON (24338-310-10) / 10 mL in 1 VIAL, SINGLE-DOSEMarketed from Oct 20, 2025 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- FeraBright
- Generic name (nonproprietary)
- ferumoxytol
- Active ingredients
- Ferumoxytol — 30 mg/mL
- Dosage form
- Injection
- Route
- Intravenous
- Labeler
- Azurity Pharmaceuticals, Inc.NDC labeler code 24338
- Product type
- Prescription drug
- Marketing category
- NDA — New Drug ApplicationApplication NDA 219868
- Marketing start
- Listing expires
- Other FDA classes
- Iron (Chemical structure)
- Identifiers
- Product ID 24338-310_ac5e7507-8e66-4da5-abd9-75ae80369b9fSPL ID ac5e7507-8e66-4da5-abd9-75ae80369b9fSPL set ID ac666008-a14f-43b4-9d06-ec70f45a4234UNII R8DG7T2D3AUPC 0324338510179, 0324338310106
- Pharmacologic class
- Parenteral Iron Replacement
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.
- Administration
Drug administration (CPT 96360–96549)
When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.
- NDC on a medical claim
N424338031010followed by a unit qualifier and the quantityPackage 24338-0310-10. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective . This label includes a boxed warning.
Indications (excerpt from the label)
FERABRIGHT is indicated for magnetic resonance imaging (MRI) of the brain in adults with known or suspected malignant neoplasms in the brain to visualize lesions with a disrupted blood-brain barrier. FERABRIGHT is an iron-based contrast agent indicated for magnetic resonance imaging (MRI) of the brain in adults with known or suspected malignant neoplasms in the brain to visualize lesions with a disrupted blood-brain barrier.
Excerpt only. Read the full label for complete information.
About NDC 24338-310
- What is NDC 24338-310?
- 24338-310 is the product NDC for FeraBright (ferumoxytol), Ferumoxytol 30 mg/mL injection, listed with the FDA by Azurity Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- FeraBright (Ferumoxytol).
- What is the active ingredient?
- Ferumoxytol.
- Who is the labeler?
- Azurity Pharmaceuticals, Inc., NDC labeler code 24338. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for FeraBright?
- 1 other product NDC are listed under this name. See all FeraBright NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other FeraBright products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| FeraBrightferumoxytol | Ferumoxytol 30 mg/mL | InjectionIntravenous | Azurity Pharmaceuticals, Inc. | 24338-510 | 24338-0510-17 |
Other NDCs under NDA 219868
Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.
| Product | Strength | Form · route | Labeler | Product NDC |
|---|---|---|---|---|
| FeraBrightferumoxytol | Ferumoxytol 30 mg/mL | InjectionIntravenous | Azurity Pharmaceuticals, Inc. | 24338-510 |