Medicinal Products

Lenalidomid Grindeks 20 mg tvrde kapsule

Name Lenalidomid Grindeks 20 mg tvrde kapsule
Marketing Authorisation Number HR-H-537202799
Active Substance lenalidomid amonijev klorid
Composition jedna kapsula sadrži 20 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-530-09/23-02/198
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
Vodic za zdravstvene radnike, verzija 5, travanj 2025
Obrazac za prijavu trudnoće, verzija 3, travanj 2025
Obrazac potvrde bolesnice u reproduktivnoj dobi, verzija 1 travanj 2025
Obrazac potvrde bolesnice koja nije u reproduktivnoj dobi, verzija 1 travanj 2025
Obrazac potvrde muškog bolesnika, verzija 1, travanj 2025
Educational materials
for patients / caregivers
Kartica za bolesnika, verzija 4, travanj 2025
Vodic za bolesnice u reproduktivnoj dobi i njihove partnere, verzija 1 travanj 2025
Vodic za bolesnice koje nisu u reproduktvnoj dobi, verzija 1 travanj 2025
Vodic za muške bolesnike, verzija1, travanj 2025

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