Humira Kit
NDC Package 0074-0243-71

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

Humira (adalimumab) kits is adalimumab is used to reduce pain and swelling due to certain types of arthritis (such as rheumatoid, psoriatic, juvenile idiopathic, ankylosing spondylitis). This formulation utilizes a kit delivery system. Marketed by Abbvie Inc., this product is identified by NDC 0074-0243 and is authorized under FDA application BLA125057.

Identification & Billing

NDC Package Code
0074-0243-71
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
11-Digit Billing Format
00074024371
RxNorm Crosswalk
  • RxCUI: 1594352 - {6 (0.8 ML adalimumab 50 MG/ML Prefilled Syringe [Humira]) } Pack [Humira Pediatric Crohn's Disease Starter Package (6 count)]
  • RxCUI: 1594352 - Humira Pediatric Crohn's Disease Starter Package (6 count)
  • RxCUI: 1594352 - Humira Pediatric Crohn's Disease Starter Pack 40 MG/0.8 ML Prefilled Syringe (6 count)
  • RxCUI: 1594357 - {3 (0.8 ML adalimumab 50 MG/ML Prefilled Syringe) } Pack
  • RxCUI: 1594357 - adalimumab pediatric starter pack 40 MG/0.8 ML Prefilled Syringe (3 count)

Clinical Specifications

Proprietary Name
Humira
Non-Proprietary Name
Adalimumab
Dosage Form
Kit - A packaged collection of related material.
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).

Regulatory & Marketing

Labeler Name
Abbvie Inc.
Product Type
Human Prescription Drug
FDA Application #
BLA125057
Marketing Category
BLA - A product marketed under an approved Biologic License Application.
Start Marketing Date
11-23-2015
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
Yes

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0074-0243). Click a package code to view its specific billing and regulatory data.

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

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 0074-0243-71 identifies a specific commercial 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, a human prescription drug labeled by Abbvie Inc.. This kit is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Abbvie Inc. on November 23, 2015. The current certification is valid through December 31, 2027.

What are the primary indications for this medication?

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).

How is this Abbvie Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00074024371. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (4-4-2)
0074-0243-71
11-Digit CMS (5-4-2)
00074-0243-71

Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.