NDC Package 0409-9966-01 Belimumab

Injection, Powder, Lyophilized, For Solution - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
0409-9966-01
Package Description:
192 VIAL in 1 PACKAGE / 5 mL in 1 VIAL (0409-9966-11)
Product Code:
Non-Proprietary Name:
Belimumab
Substance Name:
Belimumab
Usage Information:
This medication is used to treat a certain type of lupus, systemic lupus erythematosus, in patients who are receiving other lupus medicines. It works by binding to a protein (found in high levels in patients with active lupus) in the blood and limiting the activity of the protein. It helps decrease the symptoms of lupus. Belimumab is a type of medication called a monoclonal antibody.
11-Digit NDC Billing Format:
00409996601
Product Type:
Drug For Further Processing
Labeler Name:
Hospira, Inc.
Dosage Form:
Injection, Powder, Lyophilized, For Solution - A dosage form intended for the solution prepared by lyophilization ("freeze drying"), a process which involves the removal of water from products in the frozen state at extremely low pressures; this is intended for subsequent addition of liquid to create a solution that conforms in all respects to the requirements for Injections.
Active Ingredient(s):
Sample Package:
N/A
Marketing Category:
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date:
03-10-2014
Listing Expiration Date:
12-31-2024
Exclude Flag:
N
Unfinished Product:
Yes
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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Frequently Asked Questions

What is NDC 0409-9966-01?

The NDC Packaged Code 0409-9966-01 is assigned to an UNFINISHED drug package of 192 vial in 1 package / 5 ml in 1 vial (0409-9966-11) of Belimumab, drug for further processing labeled by Hospira, Inc.. The product's dosage form is injection, powder, lyophilized, for solution and is administered via form.

Is NDC 0409-9966 included in the NDC Directory?

Yes, Belimumab is an UNFINISHED PRODUCT with code 0409-9966 that is active and included in the NDC Directory. The product was first marketed by Hospira, Inc. on March 10, 2014 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0409-9966-01?

The 11-digit format is 00409996601. 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
4-4-20409-9966-015-4-200409-9966-01