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PRODUCT DETAIL

Skyrizi 150 mg injekčný roztok v naplnenom pere

Code 7772D
MA number EU/1/19/1361/002
Product Form: sol inj 1x1 ml/150 mg (pero napl.)
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
L04AC Interleukin inhibitors
L04AC18 Risankizumab
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: 26.04.2019
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 16.01.2024
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