Lenalidomid Grindeks 5 mg tvrde kapsule
Name | Lenalidomid Grindeks 5 mg tvrde kapsule |
---|---|
Marketing Authorisation Number | HR-H-448325115 |
Active Substance | lenalidomid amonijev klorid |
Composition | jedna kapsula sadrži 5 mg lenalidomida (u obliku lenalidomid amonijevog klorida) |
Pharmaceutical Form | kapsula, tvrda |
Manufacturer | Grindeks AS, Riga, Latvija |
Marketing Authorisation Holder | AS Grindeks, Krustpils iela 53, Riga, Latvija |
Marketing Authorisation Date | 30.10.2024 |
MA Period of Validity | unlimited |
Classification Number | UP/I-530-09/23-02/194 |
Registration Number | 381-12-01/70-24-03 |
Prescription | Medicinal product subject to medical prescription |
Type of prescription | ograničeni recept |
Distribution | Supply through pharmacies (community) |
Advertising to general public | not allowed |
ATC Code | L04AX04 |
Marketing status | nije stavljeno u promet |
SmPC | download |
PL | download |
Public Assessment Report | download |
Summary of risk management plan | download |
Educational materials for healthcare professionals |
Vodič za zdravstvene radnike, verzija 4 Obrazac za prijavu trudnoće, verzija 2 Obrazac pristanka bolesnika, verzija 3 |
Educational materials for patients / caregivers |
Vodič za bolesnike, verzija 4 Kartica za bolesnika, verzija 3 |