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  5. NDC Package Code: 0074-9374-71 Humira

NDC Package 0074-9374-71 Humira

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
0074-9374-71
Package Description:
2 KIT in 1 CARTON / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .4 mL in 1 SYRINGE * 1 mL in 1 PACKET
Product Code:
0074-9374
Proprietary Name:
Humira
Usage Information:
Adalimumab is used to reduce pain and swelling due to certain types of arthritis (such as rheumatoid, psoriatic, juvenile idiopathic, ankylosing spondylitis). This medication is also used to treat certain skin disorders (such as plaque-type psoriasis, hidradenitis suppurativa). It works by blocking a protein (tumor necrosis factor or TNF) found in the body's immune system that causes joint swelling and damage in arthritis as well as red scaly patches in psoriasis. Adalimumab belongs to a class of drugs known as TNF blockers. By reducing joint swelling, this medication helps to reduce further joint damage and preserve joint function. Adalimumab is also used to treat certain bowel conditions (Crohn's disease, ulcerative colitis) and a certain eye disease (uveitis).
11-Digit NDC Billing Format:
00074937471
NDC to RxNorm Crosswalk:
Labeler Name:
Abbvie Inc.
Sample Package:
Yes
FDA Application Number:
BLA125057
Marketing Category:
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date:
02-21-2008
End Marketing Date:
01-31-2021
Listing Expiration Date:
01-31-2021
Exclude Flag:
D
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
0074-9374-022 KIT in 1 CARTON / 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY / .4 mL in 1 SYRINGE * 1 mL in 1 PACKET

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 0074-9374-71?

The NDC Packaged Code 0074-9374-71 is assigned to a package of 2 kit in 1 carton / 1 kit in 1 kit * 1 syringe in 1 tray / .4 ml in 1 syringe * 1 ml in 1 packet of Humira, labeled by Abbvie Inc.. The product's dosage form is and is administered via form.

Is NDC 0074-9374 included in the NDC Directory?

No, Humira with product code 0074-9374 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Abbvie Inc. on February 21, 2008 and its listing in the NDC Directory is set to expire on January 31, 2021 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0074-9374-71?

The 11-digit format is 00074937471. 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 4-4-2 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
4-4-20074-9374-715-4-200074-9374-71