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 |
