Sitagliptin/Metformin hydrochloride SUN
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 | Sitagliptin/Metformin hydrochloride SUN |
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Active Substance | sitagliptinfumarat metforminklorid |
Prescription | na recept |
Type of prescription | ponovljivi recept |
Distribution | u ljekarni |
ATC Code | A10BD07 |
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 |