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  5. NDC Package Code: 0173-0896-01 Blenrep

NDC Package 0173-0896-01 Blenrep

Belantamab Injection, Powder, Lyophilized, For Solution Intravenous - 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:
0173-0896-01
Package Description:
1 VIAL in 1 CARTON / 2 mL in 1 VIAL
Product Code:
0173-0896
Proprietary Name:
Blenrep
Non-Proprietary Name:
Belantamab
Substance Name:
Belantamab Mafodotin
Usage Information:
BLENREP is indicated for the treatment of adults with relapsed or refractory multiple myeloma who have received at least 4 prior therapies, including an anti-CD38 monoclonal antibody, a proteasome inhibitor, and an immunomodulatory agent.This indication is approved under accelerated approval based on response rate [see Clinical Studies (14)]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in a confirmatory trial(s).
11-Digit NDC Billing Format:
00173089601
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: 2387838 - belantamab mafodotin-blmf 100 MG Injection
  • RxCUI: 2387843 - BLENREP 100 MG Injection
  • RxCUI: 2387843 - belantamab mafodotin-blmf 100 MG Injection [Blenrep]
  • RxCUI: 2387843 - Blenrep 100 MG Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Glaxosmithkline Llc
    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.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • BELANTAMAB MAFODOTIN 50 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    BLA761158
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    08-05-2020
    End Marketing Date:
    06-30-2024
    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 0173-0896-01?

    The NDC Packaged Code 0173-0896-01 is assigned to a package of 1 vial in 1 carton / 2 ml in 1 vial of Blenrep, a human prescription drug labeled by Glaxosmithkline Llc. The product's dosage form is injection, powder, lyophilized, for solution and is administered via intravenous form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 0173-0896 included in the NDC Directory?

    Yes, Blenrep with product code 0173-0896 is active and included in the NDC Directory. The product was first marketed by Glaxosmithkline Llc on August 05, 2020.

    What is the NDC billing unit for package 0173-0896-01?

    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 0173-0896-01?

    The 11-digit format is 00173089601. 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
    4-4-20173-0896-015-4-200173-0896-01