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PRODUCT DETAIL

GOBIVAZ 50 mg injekčný roztok naplnený v injekčnom pere

Code 2201F
MA number EU/1/25/1988/001
Product Form: sol ira 1x0,5 ml/50 mg (pero napl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: ADVANZ PHARMA LIMITED, Ireland
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L04 Immunosuppressants
L04A Immunosuppressants
L04AB Tumor necrosis factor alpha (TNF-alpha) inhibitors
L04AB06 Golimumab
Shelf life: 24
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 10(4) similar biological application
MA issued: 17.11.2025
Validity: 17.11.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 12.12.2025
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