Deferasiroks Pliva 250 mg tablete za oralnu suspenziju
| Name | Deferasiroks Pliva 250 mg tablete za oralnu suspenziju |
|---|---|
| Marketing Authorisation Number | HR-H-971006372 |
| Active Substance | deferasiroks |
| Composition | svaka tableta za oralnu suspenziju sadrži 250 mg deferasiroksa |
| Pharmaceutical Form | tableta za oralnu suspenziju |
| Manufacturer | Merckle GmbH, Blaubeuren, Njemačka
Pliva Hrvatska d.o.o., Zagreb, Hrvatska |
| Marketing Authorisation Holder | Pliva Hrvatska d.o.o., Prilaz baruna Filipovića 25, Zagreb, Hrvatska |
| Marketing Authorisation Date | 07.04.2022 |
| MA Period of Validity | unlimited |
| MA Revocation Date | 08.01.2026* |
| Classification Number | UP/I-530-09/21-02/196 |
| Registration Number | 381-12-01/154-22-02 |
| Prescription | Medicinal product subject to medical prescription |
| Type of prescription | Medicinal product subject to restricted medical prescription |
| Distribution | Supply through pharmacies (community) |
| Advertising to general public | not allowed |
| ATC Code | V03AC03 |
| Marketing status | Never marketed |
| SmPC | download |
| PL | download |
| Public Assessment Report | download |
| Educational materials for healthcare professionals |
Vodič za zdravstvene radnike, verzija 2 |
| Educational materials for patients / caregivers |
Vodič za bolesnike, verzija 2 |
*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Marketing authorisation has been revoked by request of the marketing authorisation holder.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.
