NDC Package 63020-198-30 Alunbrig

Brigatinib Kit - View Billable Units, 11-Digit Format, RxNorm

Package Information
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:

63020-198-30

Package Description:

1 KIT in 1 CARTON * 7 TABLET, FILM COATED in 1 BOTTLE (63020-090-07) * 23 TABLET, FILM COATED in 1 BOTTLE (63020-180-23)

Product Code:

63020-198

Proprietary Name:

Alunbrig

Non-Proprietary Name:

Brigatinib

Usage Information:

Brigatinib is used to treat a certain type of lung cancer (non-small cell lung cancer). It works by slowing or stopping the growth of cancer cells.

11-Digit NDC Billing Format:

63020019830

Billing Unit:

EA - Billing unit of "each" is used when the product is dispensed in discreet units.

NDC to RxNorm Crosswalk:

RxCUI: 1921222 - brigatinib 30 MG Oral Tablet
RxCUI: 1921228 - ALUNBRIG 30 MG Oral Tablet
RxCUI: 1921228 - brigatinib 30 MG Oral Tablet [Alunbrig]
RxCUI: 1921228 - Alunbrig 30 MG Oral Tablet
RxCUI: 1925494 - brigatinib 90 MG Oral Tablet

Product Type:

Human Prescription Drug

Labeler Name:

Takeda Pharmaceuticals America, Inc.

Dosage Form:

Kit - A packaged collection of related material.

Sample Package:

FDA Application Number:

NDA208772

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

04-28-2017

Listing Expiration Date:

12-31-2025

Exclude Flag:

Code Structure:

63020 - Takeda Pharmaceuticals America, Inc.
- 63020-198 - Alunbrig
  - 63020-198-30 - 1 KIT in 1 CARTON * 7 TABLET, FILM COATED in 1 BOTTLE (63020-090-07) * 23 TABLET, FILM COATED in 1 BOTTLE (63020-180-23)

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 63020-198-30?

The NDC Packaged Code 63020-198-30 is assigned to a package of 1 kit in 1 carton * 7 tablet, film coated in 1 bottle (63020-090-07) * 23 tablet, film coated in 1 bottle (63020-180-23) of Alunbrig, a human prescription drug labeled by Takeda Pharmaceuticals America, Inc.. The product's dosage form is kit and is administered via form.

Is NDC 63020-198 included in the NDC Directory?

Yes, Alunbrig with product code 63020-198 is active and included in the NDC Directory. The product was first marketed by Takeda Pharmaceuticals America, Inc. on April 28, 2017 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 NDC billing unit for package 63020-198-30?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

What is the 11-digit format for NDC 63020-198-30?

The 11-digit format is 63020019830. 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	63020-198-30	5-4-2	63020-0198-30

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