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PRODUCT DETAIL

Olumiant 1 mg filmom obalené tablety

Code 4937E
MA number EU/1/16/1170/017
Product Form: tbl flm 14x1 mg (blis.PVC/PE/PCTFE/Al)
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
L04AA Selective immunosuppressants
L04AA37 Baricitinib
Shelf life: 36
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 13.02.2017
SmPC + PL: European Medicines Agency's database
Dokument: Olumiant_Karta pacienta.pdf  
Dokument: Olumiant_informacie pre zdravotnickych pracovnikov_dermatologia.pdf  
Dokument: Olumiant_informacie pre zdravotnickych pracovnikov_reumatologia.pdf  
Safety feature Yes
Data update: 03.11.2023
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