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  5. NDC Package Code: 78206-148-01 Ontruzant

NDC Package 78206-148-01 Ontruzant

Kit Intravenous - 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:
78206-148-01
Package Description:
1 KIT in 1 CARTON * 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, MULTI-DOSE * 1 INJECTION, SOLUTION in 1 VIAL
Product Code:
78206-148
Proprietary Name:
Ontruzant
Non-Proprietary Name:
Ontruzant
Usage Information:
None.
11-Digit NDC Billing Format:
78206014801
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 2289227 - trastuzumab-dttb 150 MG Injection
  • RxCUI: 2289232 - Ontruzant 150 MG Injection
  • RxCUI: 2289232 - trastuzumab-dttb 150 MG Injection [Ontruzant]
  • RxCUI: 2289234 - trastuzumab-dttb 420 MG in 20 ML Injectable Solution
  • RxCUI: 2289234 - trastuzumab-dttb 21 MG/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Organon Llc
    Dosage Form:
    Kit - A packaged collection of related material.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Sample Package:
    No
    FDA Application Number:
    BLA761100
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    06-01-2021
    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 78206-148-01?

    The NDC Packaged Code 78206-148-01 is assigned to a package of 1 kit in 1 carton * 1 injection, powder, lyophilized, for solution in 1 vial, multi-dose * 1 injection, solution in 1 vial of Ontruzant, a human prescription drug labeled by Organon Llc. The product's dosage form is kit and is administered via intravenous form.

    Is NDC 78206-148 included in the NDC Directory?

    Yes, Ontruzant with product code 78206-148 is active and included in the NDC Directory. The product was first marketed by Organon Llc on June 01, 2021 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 78206-148-01?

    The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units.

    What is the 11-digit format for NDC 78206-148-01?

    The 11-digit format is 78206014801. 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
    5-3-278206-148-015-4-278206-0148-01