NDC Package 72606-042-02 Avtozma

Tocilizumab Injection, Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

72606-042-02

Package Description:

4 VIAL, SINGLE-DOSE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-DOSE

Product Code:

72606-042

Proprietary Name:

Avtozma

Non-Proprietary Name:

Tocilizumab

Substance Name:

Tocilizumab

Usage Information:

This medication is used alone or with other medications to treat moderate to severe rheumatoid arthritis in adults. It is also used to treat rheumatoid arthritis in children (such as systemic juvenile idiopathic arthritis-SJIA, polyarticular juvenile idiopathic arthritis-PJIA). It helps to reduce pain and swelling due to rheumatoid arthritis. Tocilizumab may also be used to treat a reaction (Cytokine Release Syndrome-CRS) caused by certain cancer treatments. Tocilizumab belongs to a class of drugs known as Interleukin-6 (IL-6) blockers. It works by blocking IL-6, a substance made by the body that causes swelling (inflammation).

11-Digit NDC Billing Format:

72606004202

NDC to RxNorm Crosswalk:

RxCUI: 2705425 - tocilizumab-anoh 162 MG in 0.9 ML Prefilled Syringe
RxCUI: 2705425 - 0.9 ML tocilizumab-anoh 180 MG/ML Prefilled Syringe
RxCUI: 2705425 - tocilizumab-anoh 162 MG per 0.9 ML Prefilled Syringe
RxCUI: 2705425 - tocilizumab-anoh 180 MG/ML per 0.9 ML Prefilled Syringe
RxCUI: 2705432 - Avtozma 162 MG in 0.9 ML Prefilled Syringe

Product Type:

Human Prescription Drug

Labeler Name:

Celltrion Usa, Inc.

Dosage Form:

Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.

Administration Route(s):

Intravenous - Administration within or into a vein or veins.

Active Ingredient(s):

TOCILIZUMAB 80 mg/4mL

Pharmacologic Class(es):

Sample Package:

FDA Application Number:

BLA761420

Marketing Category:

BLA - A product marketed under an approved Biologic License Application.

Start Marketing Date:

01-26-2025

Listing Expiration Date:

12-31-2026

Exclude Flag:

Code Structure:

72606 - Celltrion Usa, Inc.
- 72606-042 - Avtozma
  - 72606-042-02 - 4 VIAL, SINGLE-DOSE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-DOSE

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 Code	Package Description
72606-042-01	1 VIAL, SINGLE-DOSE in 1 CARTON / 4 mL in 1 VIAL, SINGLE-DOSE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 72606-042-02?

The NDC Packaged Code 72606-042-02 is assigned to a package of 4 vial, single-dose in 1 carton / 4 ml in 1 vial, single-dose of Avtozma, a human prescription drug labeled by Celltrion Usa, Inc.. The product's dosage form is injection, solution and is administered via intravenous form.

Is NDC 72606-042 included in the NDC Directory?

Yes, Avtozma with product code 72606-042 is active and included in the NDC Directory. The product was first marketed by Celltrion Usa, Inc. on January 26, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 72606-042-02?

The 11-digit format is 72606004202. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	72606-042-02	5-4-2	72606-0042-02

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