Fintepla
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 | Fintepla |
---|---|
Active Substance | fenfluraminklorid |
Prescription | na recept |
Type of prescription | ograničeni recept |
Distribution | u ljekarni |
ATC Code | N03AX26 |
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 healthcare professionals |
Vodič za propisivače, verzija 2 |
Educational materials for patients / caregivers |
Vodič za bolesnike, verzija 2 |