Zoledronatna kiselina 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 | Zoledronatna kiselina Hospira |
|---|---|
| Active Substance | zoledronatna kiselina hidrat |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | ograničeni recept (koncentrat za otopinu za infuziju, otopina za infuziju) |
| Distribution | Supply through pharmacies (community) |
| ATC Code | M05BA08 |
| Marketing status | nije stavljeno u promet |
| 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 |
