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  5. NDC Package Code: 82737-073-01 Aphexda

NDC Package 82737-073-01 Aphexda

Motixafortide Injection, Powder, Lyophilized, For Solution Subcutaneous - 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:
82737-073-01
Package Description:
1 VIAL, GLASS in 1 CARTON / 1.7 mL in 1 VIAL, GLASS
Product Code:
82737-073
Proprietary Name:
Aphexda
Non-Proprietary Name:
Motixafortide
Substance Name:
Motixafortide Acetate
Usage Information:
APHEXDA is indicated in combination with filgrastim (G-CSF) to mobilize hematopoietic stem cells to the peripheral blood for collection and subsequent autologous transplantation in patients with multiple myeloma.
11-Digit NDC Billing Format:
82737007301
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: 2664901 - motixafortide 62 MG Injection
  • RxCUI: 2664901 - motixafortide 62 MG (as motixafortide acetate) Injection
  • RxCUI: 2664906 - APHEXDA 62 MG Injection
  • RxCUI: 2664906 - motixafortide 62 MG Injection [Aphexda]
  • RxCUI: 2664906 - Aphexda 62 MG (as motixafortide acetate) Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Biolinerx Usa Inc
    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):
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
    • Active Ingredient(s):
  • MOTIXAFORTIDE ACETATE 62 mg/1.7mL
    • Sample Package:
    No
    FDA Application Number:
    NDA217159
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    09-08-2023
    Listing Expiration Date:
    12-31-2024
    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 82737-073-01?

    The NDC Packaged Code 82737-073-01 is assigned to a package of 1 vial, glass in 1 carton / 1.7 ml in 1 vial, glass of Aphexda, a human prescription drug labeled by Biolinerx Usa Inc. The product's dosage form is injection, powder, lyophilized, for solution and is administered via subcutaneous form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

    Is NDC 82737-073 included in the NDC Directory?

    Yes, Aphexda with product code 82737-073 is active and included in the NDC Directory. The product was first marketed by Biolinerx Usa Inc on September 08, 2023 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 82737-073-01?

    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 82737-073-01?

    The 11-digit format is 82737007301. 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
    5-3-282737-073-015-4-282737-0073-01