[Skip navigation]FDA Logo links to FDA home page
Center for Drug Evaluation and Research, U.S. Food and Drug AdministrationU.S. Food and Drug AdministrationCenter for Drug Evaluation and Research
 HHS Logo links to Department of Health and Human Services website
Drugs at FDA: FDA Approved Drug Products. Links to Initial Search Page FAQ  |  Instructions  |  Glossary  |  Contact Us  |  CDER Home 
Start Over (Drugs@FDA Home)

Drug Details
Drug Name(s) HUMIRA (Brand Name Drug)
FDA Application No. (BLA) 125057
Active Ingredient(s) ADALIMUMAB
Company ABBOTT
Original Approval or Tentative Approval Date December 31, 2002

  • There are no Therapeutic Equivalents

Products on Application (BLA) #125057
    Click on a column header to re-sort the table:

Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing
Status
RLD
TE
Code
HUMIRA  ADALIMUMAB  40MG/0.8ML  SYRINGE  Prescription  No None  
HUMIRA  ADALIMUMAB  40MG/0.8ML  VIAL  Prescription  No None  

Back to Top | Back to Previous Page | Back to Drugs@FDA Home

Disclaimer
CDER Home Page | Contact CDER | What's New @ CDER
FDA Home Page | FDA A-Z Index | Contact FDA | Privacy | Accessibility | HHS Home Page
FDA/Center for Drug Evaluation and Research
Office of Training and Communications
Division of Information Services
Update Frequency: Daily