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PRODUCT DETAIL

Humira 40 mg/0,8 ml injekčný roztok

Code 40793
MA number EU/1/03/256/001
Product Form: sol inj 2x0,8 ml/40 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AB Tumor necrosis factor alpha (TNF-alpha) inhibitors
L04AB04 Adalimumab
Shelf life: 24
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 08.09.2003
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 24.08.2018
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