Adrienne 0,02 mg /3 mg filmom obložene tablete
| Name | Adrienne 0,02 mg /3 mg filmom obložene tablete |
|---|---|
| Marketing Authorisation Number | HR-H-444853096 |
| Active Substance | etinilestradiol drospirenon |
| Composition | svaka filmom obložena tableta sadrži 0,02 mg etinilestradiola i 3 mg drospirenona |
| Pharmaceutical Form | filmom obložena tableta |
| Manufacturer | Jadran Galenski laboratorij d.d., Rijeka, Hrvatska
Laboratorios Leon Farma S.A., Villaquialambre, Leon, Španjolska |
| Marketing Authorisation Holder | Jadran Galenski laboratorij d.d., Svilno 20, Rijeka, Hrvatska |
| Marketing Authorisation Date | 14.02.2022 |
| MA Period of Validity | unlimited |
| MA Revocation Date | 19.01.2026* |
| Classification Number | UP/I-530-09/21-02/65 |
| Registration Number | 381-12-01/154-22-07 |
| 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 | G03AA12 |
| Marketing status | Not marketed |
| SmPC | download |
| PL | download |
| Public Assessment Report | download |
| Educational materials for healthcare professionals |
Lista provjere za propisivača + rp s informacijama za korisnicu, ver 1 |
| Educational materials for patients / caregivers |
Kartica sa informacijama za korisnicu, verzija 1 |
*Note
Marketing authorisation has been revoked by request of the marketing authorisation holder. In accordance with Article 113 of Medicinal Products Act (Official Gazette No. 76/13), only a medicinal product in respect of which a marketing authorisation has been granted by the Agency for Medicinal Products and Medical Devices or the European Commision, and a medicinal product in respect of which an authorisation for parallel import or parallel distribution has been granted may be placed on the market of the Republic of Croatia. By way of derogation from this provision, a batch of medicinal product may be on the market for no longer than 18 months following the expiry of revocation of the marketing authorisation, unless its shelf life expires first.
