Medicinal Products

Daylette 3 mg/0,02 mg filmom obložene tablete

Name Daylette 3 mg/0,02 mg filmom obložene tablete
Marketing Authorisation Number HR-H-141142856
Active Substance drospirenon
etinilestradiol
Composition jedna filmom obložena tableta sadrži 3 mg drospirenona i 0,02 mg etinilestradiola
Pharmaceutical Form filmom obložena tableta
Packaging [MA Number for Packaging] 28 tableta u blisteru, u kutiji  [HR-H-141142856-01]
84 tablete u blisteru, u kutiji  [HR-H-141142856-02]
168 tableta u blisteru, u kutiji  [HR-H-141142856-03]
364 tableta u blisteru, u kutiji  [HR-H-141142856-04]
Manufacturer Gedeon Richter Plc., Budimpešta, Mađarska
Marketing Authorisation Holder Gedeon Richter Plc., Gyömrői út 19-21, Budimpešta, Mađarska
Marketing Authorisation Date 14.05.2018
MA Period of Validity 14.05.2023
Classification Number UP/I-530-09/17-01/226
Registration Number 381-12-01/70-18-04
Prescription na recept
Type of prescription ponovljivi recept
Distribution u ljekarni
Advertising to general public zabranjeno
ATC Code G03AA12
Medicinal product marketed in the Croatia Da
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