1. Home
  2. Labeler Index
  3. Genentech, Inc.
  4. 50242-176
  5. NDC Package Code: 50242-176-01 Tnkase

NDC Package 50242-176-01 Tnkase

Tenecteplase Kit - 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:
50242-176-01
Package Description:
1 KIT in 1 CARTON * 1 VIAL, SINGLE-USE in 1 CARTON (50242-037-06) / 50 mg in 1 VIAL, SINGLE-USE * 1 VIAL, SINGLE-USE in 1 CARTON (50242-901-09) / 10 mL in 1 VIAL, SINGLE-USE
Product Code:
50242-176
Proprietary Name:
Tnkase
Non-Proprietary Name:
Tenecteplase
Usage Information:
TNKase® is indicated to reduce the risk of death associated with acute ST elevation myocardial infarction (STEMI).
11-Digit NDC Billing Format:
50242017601
NDC to RxNorm Crosswalk:
  • RxCUI: 284422 - TNKase 50 MG Injection
  • RxCUI: 284422 - tenecteplase 50 MG Injection [Tnkase]
  • RxCUI: 284422 - Tnkase 50 MG Injection
  • RxCUI: 313212 - tenecteplase 50 MG Injection
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Genentech, Inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    BLA103909
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    01-05-2024
    Listing Expiration Date:
    12-31-2025
    Exclude Flag:
    N
    Code Structure:
    • 50242 - Genentech, Inc.
      • 50242-176 - Tnkase
        • 50242-176-01 - 1 KIT in 1 CARTON * 1 VIAL, SINGLE-USE in 1 CARTON (50242-037-06) / 50 mg in 1 VIAL, SINGLE-USE * 1 VIAL, SINGLE-USE in 1 CARTON (50242-901-09) / 10 mL in 1 VIAL, SINGLE-USE

    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 50242-176-01?

    The NDC Packaged Code 50242-176-01 is assigned to a package of 1 kit in 1 carton * 1 vial, single-use in 1 carton (50242-037-06) / 50 mg in 1 vial, single-use * 1 vial, single-use in 1 carton (50242-901-09) / 10 ml in 1 vial, single-use of Tnkase, a human prescription drug labeled by Genentech, Inc.. The product's dosage form is kit and is administered via form.

    Is NDC 50242-176 included in the NDC Directory?

    Yes, Tnkase with product code 50242-176 is active and included in the NDC Directory. The product was first marketed by Genentech, Inc. on January 05, 2024 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 11-digit format for NDC 50242-176-01?

    The 11-digit format is 50242017601. 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
    5-3-250242-176-015-4-250242-0176-01