Medicinal Products


The medicinal product has been authorised by the European Commission (EC) via centralised procedure in all EU Member States, based on the European Medicines Agency (EMA) experts' opinion.

Name Simponi
Active Substance golimumab
Prescription na recept
Type of prescription ograničeni recept (otopina za injekciju u napunjenoj brizgalici, otopina za injekciju u napunjenoj štrcaljki)
Distribution u ljekarni
ATC Code L04AB06
Medicinal product marketed in the Croatia Da
Summary of product characteristics (SmPC), labelling and package leaflet (PL) download
Link to the European Medicines Agency's (EMA) product information download
Link to the European Commission's (EC) decisions download
Educational materials
for patients / caregivers
Kartica s podsjetnikom za bolesnika