Emtricitabine/Tenofovir disoproxil Zentiva
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 | Emtricitabine/Tenofovir disoproxil Zentiva |
|---|---|
| Active Substance | emtricitabin tenofovirdizoproksil fosfat |
| Prescription | na recept |
| Type of prescription | ograničeni recept |
| Distribution | u ljekarni |
| ATC Code | J05AR03 |
| 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 |
