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  5. NDC Package Code: 72606-025-08 Zymfentra

NDC Package 72606-025-08 Zymfentra

Infliximab-dyyb Injection Subcutaneous - 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:
72606-025-08
Package Description:
6 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
Product Code:
72606-025
Proprietary Name:
Zymfentra
Non-Proprietary Name:
Infliximab-dyyb
Substance Name:
Infliximab
Usage Information:
This medication is used to treat certain types of arthritis (rheumatoid arthritis, arthritis of the spine, psoriatic arthritis), certain bowel diseases (Crohn's disease, ulcerative colitis), and a certain severe skin disease (chronic plaque psoriasis). In these conditions, the body's defense system (immune system) attacks healthy tissues. Infliximab works by blocking the actions of a certain natural substance (tumor necrosis factor alpha) in the body. This helps to decrease swelling (inflammation) and weaken your immune system, which slows or stops the damage from the disease. This monograph is about the following infliximab products: infliximab, infliximab-abda, infliximab-axxq, and infliximab-dyyb.
11-Digit NDC Billing Format:
72606002508
NDC to RxNorm Crosswalk:
  • RxCUI: 2675742 - inFLIXimab-dyyb 120 MG in 1 ML Pen Injector
  • RxCUI: 2675742 - 1 ML infliximab-dyyb 120 MG/ML Pen Injector
  • RxCUI: 2675742 - infliximab-dyyb 120 MG per 1 ML Pen Injector
  • RxCUI: 2675749 - Zymfentra 120 MG in 1 ML Pen Injector
  • RxCUI: 2675749 - 1 ML infliximab-dyyb 120 MG/ML Pen Injector [Zymfentra]
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Celltrion Usa 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):
  • INFLIXIMAB 120 mg/mL
    • Pharmacologic Class(es):
  • Tumor Necrosis Factor Blocker - [EPC] (Established Pharmacologic Class)
  • Tumor Necrosis Factor Receptor Blocking Activity - [MoA] (Mechanism of Action)
    • Sample Package:
    No
    FDA Application Number:
    BLA761358
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    03-01-2024
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    72606-025-011 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-022 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-034 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-046 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-051 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-062 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-091 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-102 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-114 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE
    72606-025-126 SYRINGE in 1 CARTON / 1 mL in 1 SYRINGE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 72606-025-08?

    The NDC Packaged Code 72606-025-08 is assigned to a package of 6 syringe in 1 carton / 1 ml in 1 syringe of Zymfentra, a human prescription drug labeled by Celltrion Usa Inc.. The product's dosage form is injection and is administered via subcutaneous form.

    Is NDC 72606-025 included in the NDC Directory?

    Yes, Zymfentra with product code 72606-025 is active and included in the NDC Directory. The product was first marketed by Celltrion Usa Inc. on March 01, 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 11-digit format for NDC 72606-025-08?

    The 11-digit format is 72606002508. 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
    5-3-272606-025-085-4-272606-0025-08