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  5. NDC Package Code: 24338-510-17 Ferabright

NDC Package 24338-510-17 Ferabright

Ferumoxytol Injection Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
24338-510-17
Package Description:
1 VIAL, SINGLE-DOSE in 1 CARTON / 17 mL in 1 VIAL, SINGLE-DOSE
Product Code:
24338-510
Proprietary Name:
Ferabright
Non-Proprietary Name:
Ferumoxytol
Substance Name:
Ferumoxytol
Usage Information:
This medication is used to treat "iron-poor" blood (iron deficiency anemia). Ferumoxytol is a form of injectable iron that is used if you cannot take iron by mouth because of side effects or an unsuccessful response to treatment. It is also used by people who have anemia due to long-term kidney disease. Iron is an important part of your red blood cells and is needed to carry oxygen throughout the body. Many people with kidney disease cannot get enough iron from food and require injections. People with kidney disease may also need extra iron because of blood loss during kidney dialysis treatment.
11-Digit NDC Billing Format:
24338051017
Product Type:
Human Prescription Drug
Labeler Name:
Azurity Pharmaceuticals, Inc.
Dosage Form:
Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
Administration Route(s):
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s):
FERUMOXYTOL 30 mg/mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA219868
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
10-20-2025
Listing Expiration Date:
12-31-2026
Exclude Flag:
N
Code Structure:

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 24338-510-17?

The NDC Packaged Code 24338-510-17 is assigned to a package of 1 vial, single-dose in 1 carton / 17 ml in 1 vial, single-dose of Ferabright, a human prescription drug labeled by Azurity Pharmaceuticals, Inc.. The product's dosage form is injection and is administered via intravenous form.

Is NDC 24338-510 included in the NDC Directory?

Yes, Ferabright with product code 24338-510 is active and included in the NDC Directory. The product was first marketed by Azurity Pharmaceuticals, Inc. on October 20, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 24338-510-17?

The 11-digit format is 24338051017. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
5-3-224338-510-175-4-224338-0510-17