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  5. NDC Package Code: 72579-011-02 Brukinsa

NDC Package 72579-011-02 Brukinsa

Zanubrutinib Capsule Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
72579-011-02
Package Description:
1 BOTTLE, PLASTIC in 1 CARTON / 120 CAPSULE in 1 BOTTLE, PLASTIC
Product Code:
72579-011
Proprietary Name:
Brukinsa
Non-Proprietary Name:
Zanubrutinib
Substance Name:
Zanubrutinib
Usage Information:
BRUKINSA is indicated for the treatment of adult patients with mantle cell lymphoma (MCL) who have received at least one prior therapy.This indication is approved under accelerated approval based on overall response rate [see Clinical Studies (14.1)]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial.
11-Digit NDC Billing Format:
72579001102
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2262440 - zanubrutinib 80 MG Oral Capsule
  • RxCUI: 2262446 - Brukinsa 80 MG Oral Capsule
  • RxCUI: 2262446 - zanubrutinib 80 MG Oral Capsule [Brukinsa]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Beigene Usa, Inc.
    Dosage Form:
    Capsule - A solid oral dosage form consisting of a shell and a filling. The shell is composed of a single sealed enclosure, or two halves that fit together and which are sometimes sealed with a band. Capsule shells may be made from gelatin, starch, or cellulose, or other suitable materials, may be soft or hard, and are filled with solid or liquid ingredients that can be poured or squeezed.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • ZANUBRUTINIB 80 mg/1
    • Pharmacologic Class(es):
  • Bruton's Tyrosine Kinase Inhibitors - [MoA] (Mechanism of Action)
  • Kinase Inhibitor - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    NDA213217
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    11-14-2019
    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.

    Frequently Asked Questions

    What is NDC 72579-011-02?

    The NDC Packaged Code 72579-011-02 is assigned to a package of 1 bottle, plastic in 1 carton / 120 capsule in 1 bottle, plastic of Brukinsa, a human prescription drug labeled by Beigene Usa, Inc.. The product's dosage form is capsule and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 72579-011 included in the NDC Directory?

    Yes, Brukinsa with product code 72579-011 is active and included in the NDC Directory. The product was first marketed by Beigene Usa, Inc. on November 14, 2019 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 72579-011-02?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

    What is the 11-digit format for NDC 72579-011-02?

    The 11-digit format is 72579001102. 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
    5-3-272579-011-025-4-272579-0011-02