| Name |
Duodin 500 mg filmom obložene tablete |
| Marketing Authorisation Number |
HR-H-077182273 |
| Active Substance |
diosmin |
| Composition |
svaka filmom obložena tableta sadrži 500 mg mikroniziranog diosmina |
| Pharmaceutical Form |
Filmom obložena tableta |
| Manufacturer |
Laboratorios Cinfa S.A., Huarte-Pamplona, Navarra, Španjolska |
| Marketing Authorisation Holder |
Stada d.o.o., Hercegovačka 14, Zagreb, Hrvatska |
| Marketing Authorisation Date |
20.09.2022 |
| MA Period of Validity |
27.04.2027 |
| Classification Number |
UP/I-530-09/18-01/246 |
| Registration Number |
381-12-01/70-22-10 |
| Prescription |
Medicinal product subject to medical prescription |
| Type of prescription |
Medicinal product on medical prescription for renewable delivery
|
| Distribution |
Supply through pharmacies (community) |
| Advertising to general public |
not allowed |
| ATC Code |
C05CA53 |
| Marketing status |
Never marketed |
| SmPC |
download |
| PL |
download |
| Public Assessment Report |
download
|
| Summary of risk management plan |
download |
