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PRODUCT DETAIL

Bimzelx 160 mg injekčný roztok v naplnenom pere

Code 8541D
MA number EU/1/21/1575/006
Product Form: sol inj 2x1 ml/160 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
L04AC21 Bimekizumab
Shelf life: 36
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: 20.08.2021
Validity: 20.08.2026
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 09.09.2021
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