Medicinal Products

Zoledronic Acid Hospira

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 Zoledronic Acid Hospira
Active Substance zoledronatna kiselina hidrat
Prescription na recept
Type of prescription ograničeni recept (koncentrat za otopinu za infuziju, otopina za infuziju)
Distribution u ljekarni
ATC Code M05BA08
Medicinal product marketed in the Croatia Trajni prekid opskrbe
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 za bolesnika verzija 1