Humira (adalimumab)
- Region
- 🇪🇺 EU
- Active substance
- adalimumab
- Company
- AbbVie Deutschland GmbH & Co. KG
- Status
- Authorised
- Therapeutic area
- Spondylitis, Ankylosing; Arthritis, Juvenile Rheumatoid; Uveitis; Colitis, Ulcerative; Psoriasis; Arthritis, Psoriatic; Crohn Disease; Arthritis, Rheumatoid
- EU approval
- Mon 08 Sep 2003
- Application
- EMEA/H/C/000481
- ATC
- L04AB04
- Official record
- www.ema.europa.eu
Indication
Please refer to the product information document.
Regulatory milestones
No milestones recorded in the last year.
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- 🇪🇺 Halimatoz Withdrawn · Sandoz GmbH
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Information from official EMA, FDA, Federal Register and SEC records. Dates marked company-announced come from the company's own SEC filing; dates marked estimate are calculated, not official. Not investment or medical advice; always confirm on the source.