Medicinal Products

Isturisa

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 Isturisa
Active Substance osilodrostatfosfat
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
ATC Code H02CA02
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
Back