Salmeterol/flutikazon Cipla 25 mikrograma + 250 mikrograma u jednoj dozi, stlačeni inhalat, suspenzija
Name | Salmeterol/flutikazon Cipla 25 mikrograma + 250 mikrograma u jednoj dozi, stlačeni inhalat, suspenzija |
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Former Name | Salmeterol/flutikazonpropionat Momaja 25 mikrograma + 250 mikrograma u jednoj dozi, stlačeni inhalat, suspenzija |
Marketing Authorisation Number | HR-H-705296771 |
Active Substance | salmeterolksinafoat flutikazonpropionat |
Composition | svaki pojedinačni potisak salmeterol i flutikazonpropionat stlačenog inhalata, suspenzije sadrži: 25 mikrograma salmeterola (u obliku salmeterolksinafoata) i 250 mikrograma flutikazonpropionata (ispuštenih iz ventila) |
Pharmaceutical Form | stlačeni inhalat, suspenzija |
Manufacturer | S&D Pharma CZ, spol. s r.o, Pchery (Pharmos a.s. facility), Češka Orion Corporation, Orion Pharma, Espoo, Finska Orion Corporation, Orion Pharma, Salo, Finska Amring Farma S.R.L., Bukurešt, Rumunjska Cipla Europe NV, Antwerpen, Belgija |
Marketing Authorisation Holder | Cipla Europe NV, De Keyserlei 60C, Bus 1301, Antwerpen, Belgija |
Marketing Authorisation Date | 12.05.2020 |
MA Period of Validity | unlimited |
Classification Number | UP/I-530-09/18-02/310 |
Registration Number | 381-12-01/70-20-04 |
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 | R03AK06 |
Marketing status | stavljeno u promet |
Shortage status | u tijeku |
SmPC | download |
PL | download |
Public Assessment Report | download |