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PRODUCT DETAIL

Gohibic 200 mg koncentrát na infúzny roztok

Code 8992E
MA number EU/1/24/1884/001
Product Form: con inf 4x20 ml/200 mg (liek.inj.skl.)
MA Status: Ev - Valid centralised marketing authorisation under exceptional circumstances
Type of procedure: EU
MAH, country: InflaRx GmbH, Germany
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AJ Complement inhibitors
L04AJ10 Vilobelimab
Shelf life: 12
Container: glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 13.01.2025
Validity: 13.01.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 13.02.2025
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