Medicinal Products

Daylla 3 mg/0,02 mg filmom obložene tablete

Name Daylla 3 mg/0,02 mg filmom obložene tablete
Marketing Authorisation Number HR-H-320765811
Active Substance drospirenonum, ethinylestradiolum
Pharmaceutical Form filmom obložena tableta
Strength 3 mg + 0,02 mg
Packaging [MA Number for Packaging] 28 tableta u blisteru, u kutiji  [HR-H-320765811-01]
84 tablete u blisteru, u kutiji  [HR-H-320765811-02]
168 tableta u blisteru, u kutiji  [HR-H-320765811-03]
364 tablete u blisteru, u kutiji  [HR-H-320765811-04]
Manufacturer Gedeon Richter Plc., Budimpešta, Mađarska
Marketing Authorisation Holder Gedeon Richter Plc., Gyömrői út 19-21, Budimpešta, Mađarska
Marketing Authorisation Date 20.04.2016
MA Period of Validity 20.04.2021
Classification Number UP/I-530-09/15-01/130
Registration Number 381-12-01/30-16-06
Composition jedna filmom obložena tableta sadrži 3 mg drospirenona i 0,02 mg etinilestradiola
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 Ne
SmPC download
PL download
Public Assessment Report download
Educational materials
for healthcare professionals
Lista provjere za propisivača verzija 1
Educational materials
for patients / caregivers
Važne informacije za korisnice verzija 1
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