Paliperidon Teva 150 mg i 100 mg suspenzija za injekciju s produljenim oslobađanjem
| Name | Paliperidon Teva 150 mg i 100 mg suspenzija za injekciju s produljenim oslobađanjem |
|---|---|
| Marketing Authorisation Number | HR-H-146706308 |
| Active Substance | paliperidonpalmitat |
| Composition | jedna napunjena štrcaljka sadrži 234 mg paliperidonpalmitata što odgovara 150 mg paliperidona jedna napunjena štrcaljka sadrži 156 mg paliperidonpalmitata što odgovara 100 mg paliperidona |
| Pharmaceutical Form | Suspenzija za injekciju s produljenim oslobađanjem |
| Manufacturer | Actavis Group PTC ehf., Hafnarfjoerdur, Island |
| Marketing Authorisation Holder | Teva B.V., Swensweg 5, Haarlem, Nizozemska |
| Marketing Authorisation Date | 24.06.2021 |
| MA Period of Validity | 24.06.2026 |
| MA Revocation Date | 29.09.2023* |
| Classification Number | UP/I-530-09/20-01/285 |
| Registration Number | 381-12-01/70-21-02 |
| Prescription | na recept |
| Type of prescription | ograničeni recept |
| Distribution | u ljekarni |
| Advertising to general public | zabranjeno |
| ATC Code | N05AX13 |
| SmPC | download |
| PL | download |
| Public Assessment Report | download |
*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Marketing authorisation has been revoked by request of the marketing authorisation holder.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.
