NDC Package 50419-524-81 Betaseron

Interferon Beta-1b Kit - View Billable Units, 11-Digit Format, RxNorm

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:
50419-524-81
Package Description:
14 CARTON in 1 BOX / 1 KIT in 1 CARTON (50419-524-01) * 1 mL in 1 VIAL, SINGLE-USE * 1.2 mL in 1 SYRINGE
Product Code:
Proprietary Name:
Betaseron
Non-Proprietary Name:
Interferon Beta-1b
Usage Information:
This medication is used to treat multiple sclerosis (MS). Interferon is not a cure for MS, but it may help to slow disease worsening and decrease flare-ups of symptoms (such as balance problems, numbness, or weakness).
11-Digit NDC Billing Format:
50419052481
NDC to RxNorm Crosswalk:
  • RxCUI: 198360 - interferon beta-1b 0.3 MG Injection
  • RxCUI: 207059 - BETASERON 0.3 MG Injection
  • RxCUI: 207059 - interferon beta-1b 0.3 MG Injection [Betaseron]
  • RxCUI: 207059 - Betaseron 0.3 MG Injection
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Bayer Healthcare Pharmaceuticals Inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    BLA103471
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    07-09-2009
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    50419-524-055 CARTON in 1 BOX / 1 KIT in 1 CARTON (50419-524-01) * 1 mL in 1 VIAL, SINGLE-USE * 1.2 mL in 1 SYRINGE
    50419-524-091 CARTON in 1 BOX / 1 KIT in 1 CARTON (50419-524-01) * 1 mL in 1 VIAL, SINGLE-USE * 1.2 mL in 1 SYRINGE
    50419-524-3514 CARTON in 1 BOX / 1 KIT in 1 CARTON (50419-524-01) * 1 mL in 1 VIAL, SINGLE-USE * 1.2 mL in 1 SYRINGE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50419-524-81?

    The NDC Packaged Code 50419-524-81 is assigned to a package of 14 carton in 1 box / 1 kit in 1 carton (50419-524-01) * 1 ml in 1 vial, single-use * 1.2 ml in 1 syringe of Betaseron, a human prescription drug labeled by Bayer Healthcare Pharmaceuticals Inc.. The product's dosage form is kit and is administered via form.

    Is NDC 50419-524 included in the NDC Directory?

    Yes, Betaseron with product code 50419-524 is active and included in the NDC Directory. The product was first marketed by Bayer Healthcare Pharmaceuticals Inc. on July 09, 2009 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 11-digit format for NDC 50419-524-81?

    The 11-digit format is 50419052481. 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
    5-3-250419-524-815-4-250419-0524-81