Actonel Combi D 35 mg filmom obložene tablete + 1000 mg / 880 IU šumeće granule
Name | Actonel Combi D 35 mg filmom obložene tablete + 1000 mg / 880 IU šumeće granule |
---|---|
Marketing Authorisation Number | HR-H-648885316 |
Active Substance | natrijev risedronat kalcijev karbonat kolekalciferol, koncentrat, prašak |
Composition | jedna filmom obložena tableta sadrži 35 mg natrijevog risedronata (što odgovara količini od 32,5 mg risedronatne kiseline); jedna vrećica šumećih granula sadrži 1000 mg kalcija (u obliku 2500 mg kalcijevog karbonata) i 22 mikrograma (880 IU) kolekalciferola (vitamin D3) |
Pharmaceutical Form | šumeće granule + filmom obložena tableta |
Manufacturer | Hermes Pharma Ges.m.b.H., Wolfsberg, Austrija |
Marketing Authorisation Holder | Zentiva k.s., U Kabelovny 130, Dolni Mecholupy, Prag 10, Češka |
Marketing Authorisation Date | 04.08.2021 |
MA Period of Validity | unlimited |
Classification Number | UP/I-530-09/18-02/100 |
Registration Number | 381-12-01/154-21-33 |
Prescription | Medicinal product subject to medical prescription |
Type of prescription | ponovljivi recept |
Distribution | Supply through pharmacies (community) |
Advertising to general public | not allowed |
ATC Code | M05BB04 |
Marketing status | trajni prekid opskrbe |
SmPC | download |
PL | download |