NDC Package 13533-645-20 Gamunex

View Billable Units, 11-Digit Format, RxNorm

Package Information
Other Packages
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory .

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:

13533-645-20

Package Description:

5 g in 1 VIAL, GLASS

Product Code:

13533-645

Proprietary Name:

Gamunex

Usage Information:

This medication is used to strengthen the body's natural defense system (immune system) to lower the risk of infection in persons with a weakened immune system. This medication is made from healthy human blood that has a high level of certain defensive substances (antibodies), which help fight infections. It is also used to increase the blood count (platelets) in persons with a certain blood disorder (idiopathic thrombocytopenia purpura-ITP). Platelets are needed to stop bleeding and form blood clots. Some immune globulin products may also be used to treat a certain type of muscle weakness problem (multifocal motor neuropathy) or a certain nerve disorder (chronic inflammatory demyelinating polyneuropathy-CIDP). Some products may also be used to prevent certain blood vessel disorders in people with Kawasaki syndrome.

11-Digit NDC Billing Format:

13533064520

Labeler Name:

Grifols Usa, Llc

Sample Package:

FDA Application Number:

BLA125046

Marketing Category:

BLA - A product marketed under an approved Biologic License Application.

Start Marketing Date:

08-27-2003

End Marketing Date:

10-22-2013

Listing Expiration Date:

10-22-2013

Exclude Flag:

Code Structure:

13533 - Grifols Usa, Llc
- 13533-645 - Gamunex
  - 13533-645-20 - 5 g in 1 VIAL, GLASS

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 Code	Package Description
13533-645-12	1 g in 1 VIAL, GLASS
13533-645-15	2.5 g in 1 VIAL, GLASS
13533-645-24	20 g in 1 VIAL, GLASS
13533-645-71	10 g in 1 VIAL, GLASS

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 13533-645-20?

The NDC Packaged Code 13533-645-20 is assigned to a package of 5 g in 1 vial, glass of Gamunex, labeled by Grifols Usa, Llc. The product's dosage form is and is administered via form.

Is NDC 13533-645 included in the NDC Directory?

The product was first marketed by Grifols Usa, Llc on August 27, 2003 and its listing in the NDC Directory is set to expire on October 22, 2013 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 13533-645-20?

The 11-digit format is 13533064520. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	13533-645-20	5-4-2	13533-0645-20

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