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  5. NDC Package Code: 50242-933-01 Tecentriq Hybreza

NDC Package 50242-933-01 Tecentriq Hybreza

Atezolizumab And Hyaluronidase-tqjs Injection Subcutaneous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. Other Packages
    4. 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:
50242-933-01
Package Description:
1 VIAL, SINGLE-DOSE in 1 BOX / 15 mL in 1 VIAL, SINGLE-DOSE
Product Code:
50242-933
Proprietary Name:
Tecentriq Hybreza
Non-Proprietary Name:
Atezolizumab And Hyaluronidase-tqjs
Substance Name:
Atezolizumab; Hyaluronidase (human Recombinant)
Usage Information:
TECENTRIQ HYBREZA is contraindicated in patients with known hypersensitivity to hyaluronidase or to any of its excipients.
11-Digit NDC Billing Format:
50242093301
Billing Unit:
ML - Billing unit of "milliliter" is used when a product is measured by its liquid volume.
NDC to RxNorm Crosswalk:
  • RxCUI: 2693892 - atezolizumab-hyaluronidase-tqjs 1875 MG / 30,000 UNT in 15 ML Injection
  • RxCUI: 2693892 - 15 ML atezolizumab-tqjs 125 MG/ML / hyaluronidase-tqjs 2000 UNT/ML Injection
  • RxCUI: 2693892 - atezolizumab-hyaluronidase-tqjs 1875 MG / 30,000 UNT per 15 ML Injection
  • RxCUI: 2693899 - Tecentriq Hybreza 1875 MG / 30,000 UNT in 15 ML Injection
  • RxCUI: 2693899 - 15 ML atezolizumab-tqjs 125 MG/ML / hyaluronidase-tqjs 2000 UNT/ML Injection [Tecentriq Hybreza]
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):
Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Active Ingredient(s):
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
BLA761347
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
09-12-2024
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 50242-933-01 HCPCS crosswalk information with package details and bill units information.

NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
50242093301J9024Inj atezolizumb 5mg hya-tqjs5 MG151375375

* Please review the disclaimer below.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
50242-933-861 VIAL, SINGLE-DOSE in 1 BOX / 15 mL in 1 VIAL, SINGLE-DOSE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 50242-933-01?

The NDC Packaged Code 50242-933-01 is assigned to a package of 1 vial, single-dose in 1 box / 15 ml in 1 vial, single-dose of Tecentriq Hybreza, a human prescription drug labeled by Genentech, Inc.. The product's dosage form is injection and is administered via subcutaneous form.

Is NDC 50242-933 included in the NDC Directory?

Yes, Tecentriq Hybreza with product code 50242-933 is active and included in the NDC Directory. The product was first marketed by Genentech, Inc. on September 12, 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 NDC billing unit for package 50242-933-01?

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 50242-933-01?

The 11-digit format is 50242093301. 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
5-3-250242-933-015-4-250242-0933-01