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  5. NDC Package Code: 44087-5000-6 Tepmetko

NDC Package 44087-5000-6 Tepmetko

Tepotinib Hydrochloride Tablet Oral - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. 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:
44087-5000-6
Package Description:
6 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK
Product Code:
44087-5000
Proprietary Name:
Tepmetko
Non-Proprietary Name:
Tepotinib Hydrochloride
Substance Name:
Tepotinib Hydrochloride
Usage Information:
TEPMETKO is indicated for the treatment of adult patients with metastatic non-small cell lung cancer (NSCLC) harboring mesenchymal-epithelial transition (MET) exon 14 skipping alterations.This indication is approved under accelerated approval based on overall response rate and duration of response [see Clinical Studies (14)]. Continued approval for this indication may be contingent upon verification and description of clinical benefit in confirmatory trial(s).
11-Digit NDC Billing Format:
44087500006
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
6 EA
NDC to RxNorm Crosswalk:
  • RxCUI: 2477266 - tepotinib 225 MG Oral Tablet
  • RxCUI: 2477266 - tepotinib 225 MG (equivalent to tepotinib HCl hydrate 250 MG) Oral Tablet
  • RxCUI: 2477272 - TEPMETKO 225 MG Oral Tablet
  • RxCUI: 2477272 - tepotinib 225 MG Oral Tablet [Tepmetko]
  • RxCUI: 2477272 - Tepmetko 225 MG (equivalent to tepotinib HCl hydrate 250 MG) Oral Tablet
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Emd Serono, Inc.
    Dosage Form:
    Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
    Administration Route(s):
  • Oral - Administration to or by way of the mouth.
    • Active Ingredient(s):
  • TEPOTINIB HYDROCHLORIDE 225 mg/1
    • Pharmacologic Class(es):
  • Kinase Inhibitor - [EPC] (Established Pharmacologic Class)
  • Mesenchymal Epithelial Transition Inhibitors - [MoA] (Mechanism of Action)
  • P-Glycoprotein Inhibitors - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    NDA214096
    Marketing Category:
    NDA - A product marketed under an approved New Drug Application.
    Start Marketing Date:
    02-03-2021
    Listing Expiration Date:
    12-31-2025
    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
    44087-5000-33 BLISTER PACK in 1 CARTON / 10 TABLET in 1 BLISTER PACK

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 44087-5000-6?

    The NDC Packaged Code 44087-5000-6 is assigned to a package of 6 blister pack in 1 carton / 10 tablet in 1 blister pack of Tepmetko, a human prescription drug labeled by Emd Serono, Inc.. The product's dosage form is tablet and is administered via oral form.This product is billed for "EA" each discreet unit and contains an estimated amount of 6 billable units per package.

    Is NDC 44087-5000 included in the NDC Directory?

    Yes, Tepmetko with product code 44087-5000 is active and included in the NDC Directory. The product was first marketed by Emd Serono, Inc. on February 03, 2021 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 NDC billing unit for package 44087-5000-6?

    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 6.

    What is the 11-digit format for NDC 44087-5000-6?

    The 11-digit format is 44087500006. 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 5-4-1 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
    5-4-144087-5000-65-4-244087-5000-06