Klopidogrel/acetilsalicilatna kiselina Viatris
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 | Klopidogrel/acetilsalicilatna kiselina Viatris |
|---|---|
| Former Name | Klopidogrel/acetilsalicilatna kiselina Mylan |
| Active Substance | klopidogrelhidrogensulfat acetilsalicilatna kiselina |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | ponovljivi recept |
| Distribution | Supply through pharmacies (community) |
| ATC Code | B01AC30 |
| 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 |
