NDC Package 50474-700-62 Cimzia

Certolizumab Pegol Kit - View Billable Units, 11-Digit Format, RxNorm

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:
Package Description:
2 KIT in 1 CARTON / 1 KIT in 1 KIT * 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASS
Product Code:
Proprietary Name:
Non-Proprietary Name:
Certolizumab Pegol
Usage Information:
This medication is used to reduce pain and swelling due to certain inflammatory conditions (such as rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, plaque psoriasis). Some brands may also be used to treat a certain type of spine condition (axial spondyloarthritis) or a certain bowel condition (Crohn's disease). Certolizumab belongs to a class of drugs known as tumor necrosis factor (TNF) blockers. It works by blocking TNF, a substance made by the body that causes inflammation.
11-Digit NDC Billing Format:
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
  • RxCUI: 795081 - certolizumab pegol 200 MG Injection
  • RxCUI: 795085 - Cimzia 200 MG Injection
  • RxCUI: 795085 - certolizumab pegol 200 MG Injection [Cimzia]
  • RxCUI: 849597 - certolizumab pegol 200 MG in 1 ML Prefilled Syringe
  • RxCUI: 849597 - 1 ML certolizumab pegol 200 MG/ML Prefilled Syringe
  • Product Type:
    Human Prescription Drug
    Labeler Name:
    Ucb, Inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    FDA Application Number:
    Marketing Category:
    BLA - A product marketed under an approved Biologic License Application.
    Start Marketing Date:
    Listing Expiration Date:
    Exclude Flag:
    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
    50474-700-612 KIT in 1 CARTON / 1 KIT in 1 KIT * 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASS

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50474-700-62?

    The NDC Packaged Code 50474-700-62 is assigned to a package of 2 kit in 1 carton / 1 kit in 1 kit * 1 ml in 1 vial, glass * 1 ml in 1 vial, glass of Cimzia, a human prescription drug labeled by Ucb, Inc.. The product's dosage form is kit and is administered via form.

    Is NDC 50474-700 included in the NDC Directory?

    Yes, Cimzia with product code 50474-700 is active and included in the NDC Directory. The product was first marketed by Ucb, Inc. on April 20, 2008 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 50474-700-62?

    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 50474-700-62?

    The 11-digit format is 50474070062. 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