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  5. NDC Package Code: 50242-150-01 Ocrevus

NDC Package 50242-150-01 Ocrevus

Ocrelizumab Injection Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    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:
50242-150-01
Package Description:
1 VIAL, SINGLE-USE in 1 CARTON / 10 mL in 1 VIAL, SINGLE-USE
Product Code:
50242-150
Proprietary Name:
Ocrevus
Non-Proprietary Name:
Ocrelizumab
Substance Name:
Ocrelizumab
Usage Information:
Ocrelizumab is used to treat certain forms of multiple sclerosis-MS (relapsing or primary progressive forms). It is not a cure for MS, but it is thought to help slow down nerve damage, reduce the number of relapses, and delay disability. Ocrelizumab belongs to a class of drugs known as monoclonal antibodies.
11-Digit NDC Billing Format:
50242015001
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 1876380 - ocrelizumab 300 MG in 10 ML Injection
  • RxCUI: 1876380 - 10 ML ocrelizumab 30 MG/ML Injection
  • RxCUI: 1876380 - ocrelizumab 300 MG per 10 ML Injection
  • RxCUI: 1876385 - Ocrevus 300 MG in 10 ML Injection
  • RxCUI: 1876385 - 10 ML ocrelizumab 30 MG/ML Injection [Ocrevus]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Genentech, Inc.
    Dosage Form:
    Injection - A sterile preparation intended for parenteral use; five distinct classes of injections exist as defined by the USP.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • OCRELIZUMAB 300 mg/10mL
    • Pharmacologic Class(es):
  • Antibodies, Monoclonal - [CS]
  • Antibodies, Monoclonal, Humanized - [CS]
  • CD20-directed Antibody Interactions - [MoA] (Mechanism of Action)
  • CD20-directed Cytolytic Antibody - [EPC] (Established Pharmacologic Class)
    • Sample Package:
    No
    FDA Application Number:
    BLA761053
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    03-28-2017
    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.

    NDC HCPCS Crosswalk

    This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

    NDC 50242-150-01 HCPCS crosswalk information with package details and bill units information.

    NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
    50242015001J2350Injection, ocrelizumab, 1 mg1 MG101300300

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50242-150-01?

    The NDC Packaged Code 50242-150-01 is assigned to a package of 1 vial, single-use in 1 carton / 10 ml in 1 vial, single-use of Ocrevus, a human prescription drug labeled by Genentech, Inc.. The product's dosage form is injection and is administered via intravenous form.

    Is NDC 50242-150 included in the NDC Directory?

    Yes, Ocrevus with product code 50242-150 is active and included in the NDC Directory. The product was first marketed by Genentech, Inc. on March 28, 2017 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 50242-150-01?

    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 50242-150-01?

    The 11-digit format is 50242015001. 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
    5-3-250242-150-015-4-250242-0150-01