NDC Package 0409-2336-13 Deferoxamine Mesylate

View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
0409-2336-13
Package Description:
10 VIAL, SINGLE-USE in 1 CARTON / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE
Product Code:
Proprietary Name:
Deferoxamine Mesylate
Usage Information:
This medication is used along with other treatments (such as causing vomiting with syrup of ipecac, stomach pumping) to treat sudden iron poisoning. It is most effective when given as soon as possible after the iron was eaten. This medication can also be used to help get rid of iron in patients with high iron levels due to many blood transfusions. Deferoxamine is an iron-binding agent that belongs to a class of drugs known as heavy metal antagonists. It works by helping the kidneys and gallbladder get rid of the extra iron. This medication is not recommended for use in children less than 3 years old (see also Precautions section).
11-Digit NDC Billing Format:
00409233613
NDC to RxNorm Crosswalk:
Labeler Name:
Hospira, Inc.
Sample Package:
No
FDA Application Number:
ANDA076019
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
03-17-2004
End Marketing Date:
03-17-2004
Listing Expiration Date:
03-17-2004
Exclude Flag:
D
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.

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Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
0409-2336-104 VIAL, SINGLE-USE in 1 CARTON / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (0409-2336-01)

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Frequently Asked Questions

What is NDC 0409-2336-13?

The NDC Packaged Code 0409-2336-13 is assigned to a package of 10 vial, single-use in 1 carton / 1 injection, powder, lyophilized, for solution in 1 vial, single-use of Deferoxamine Mesylate, labeled by Hospira, Inc.. The product's dosage form is and is administered via form.

Is NDC 0409-2336 included in the NDC Directory?

No, Deferoxamine Mesylate with product code 0409-2336 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Hospira, Inc. on March 17, 2004 and its listing in the NDC Directory is set to expire on March 17, 2004 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0409-2336-13?

The 11-digit format is 00409233613. 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 4-4-2 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
4-4-20409-2336-135-4-200409-2336-13