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  5. NDC Package Code: 44206-310-11 Alburx

NDC Package 44206-310-11 Alburx

Albumin (human) Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
44206-310-11
Package Description:
1 VIAL, GLASS in 1 CARTON / 50 mL in 1 VIAL, GLASS
Product Code:
44206-310
Proprietary Name:
Alburx
Non-Proprietary Name:
Albumin (human)
Substance Name:
Albumin Human
Usage Information:
The use of AlbuRx® 5, Albumin (Human) 5% solution is contraindicated in patients with a history of an incompatibility reaction to such preparations (see ADVERSE REACTIONS). In addition, AlbuRx® 5 may be contraindicated in patients with cardiac failure or severe anemia because of the risk of acute circulatory overload.
11-Digit NDC Billing Format:
44206031011
NDC to RxNorm Crosswalk:
Product Type:
Plasma Derivative
Labeler Name:
Csl Behring Ag
Dosage Form:
Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
Administration Route(s):
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s):
ALBUMIN HUMAN 12.5 g/250mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
BLA102366
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
01-06-2009
Listing Expiration Date:
12-31-2025
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
44206-310-251 VIAL, GLASS in 1 CARTON / 250 mL in 1 VIAL, GLASS (44206-310-90)
44206-310-501 VIAL, GLASS in 1 CARTON / 500 mL in 1 VIAL, GLASS (44206-310-91)

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 44206-310-11?

The NDC Packaged Code 44206-310-11 is assigned to a package of 1 vial, glass in 1 carton / 50 ml in 1 vial, glass of Alburx, a plasma derivative labeled by Csl Behring Ag. The product's dosage form is solution and is administered via intravenous form.

Is NDC 44206-310 included in the NDC Directory?

Yes, Alburx with product code 44206-310 is active and included in the NDC Directory. The product was first marketed by Csl Behring Ag on January 06, 2009 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 44206-310-11?

The 11-digit format is 44206031011. 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
5-3-244206-310-115-4-244206-0310-11