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  5. NDC Package Code: 0169-2080-15 Alhemo

NDC Package 0169-2080-15 Alhemo

Concizumab Injection, 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:
0169-2080-15
Package Description:
1 SYRINGE, PLASTIC in 1 CARTON / 1.5 mL in 1 SYRINGE, PLASTIC
Product Code:
0169-2080
Proprietary Name:
Alhemo
Non-Proprietary Name:
Concizumab
Substance Name:
Concizumab
Usage Information:
Alhemo is indicated for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult and pediatric patients 12 years of age and older with:•hemophilia A (congenital factor VIII deficiency) with FVIII inhibitors•hemophilia B (congenital factor IX deficiency) with FIX inhibitors
11-Digit NDC Billing Format:
00169208015
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Novo Nordisk
Dosage Form:
Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
Administration Route(s):
Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Active Ingredient(s):
CONCIZUMAB 100 mg/mL
Sample Package:
No
FDA Application Number:
BLA761315
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
02-19-2025
Listing Expiration Date:
12-31-2026
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 0169-2080-15?

The NDC Packaged Code 0169-2080-15 is assigned to a package of 1 syringe, plastic in 1 carton / 1.5 ml in 1 syringe, plastic of Alhemo, a human prescription drug labeled by Novo Nordisk. The product's dosage form is injection, solution and is administered via subcutaneous form.

Is NDC 0169-2080 included in the NDC Directory?

Yes, Alhemo with product code 0169-2080 is active and included in the NDC Directory. The product was first marketed by Novo Nordisk on February 19, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 0169-2080-15?

The contents of this package are billed per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.

What is the 11-digit format for NDC 0169-2080-15?

The 11-digit format is 00169208015. 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
4-4-20169-2080-155-4-200169-2080-15