Humira - 0074-3799-02 - (Adalimumab)

Alphabetical Index


Drug Information of Humira

Product NDC: 0074-3799
Proprietary Name: Humira
Non Proprietary Name: Adalimumab
Active Ingredient(s):    & nbsp;   Adalimumab
Administration Route(s):
Dosage Form(s): KIT
Coding System: National Drug Codes(NDC)

Labeler Information of Humira

Product NDC: 0074-3799
Labeler Name: AbbVie Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: BLA125057
Marketing Category: BLA
Start Marketing Date: 20110405

Package Information of Humira

Package NDC: 0074-3799-02
Package Description: 2 KIT in 1 CARTON (0074-3799-02) > 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY > .8 mL in 1 SYRINGE * 1 SWAB in 1 PACKET

NDC Information of Humira

NDC Code 0074-3799-02
Proprietary Name Humira
Package Description 2 KIT in 1 CARTON (0074-3799-02) > 1 KIT in 1 KIT * 1 SYRINGE in 1 TRAY > .8 mL in 1 SYRINGE * 1 SWAB in 1 PACKET
Product NDC 0074-3799
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Adalimumab
Dosage Form Name KIT
Route Name
Start Marketing Date 20110405
Marketing Category Name BLA
Labeler Name AbbVie Inc.
Substance Name
Strength Number
Strength Unit
Pharmaceutical Classes

Complete Information of Humira


General Information