Medicinal Products

Lenalidomid Aristo 10 mg tvrde kapsule

Name Lenalidomid Aristo 10 mg tvrde kapsule
Marketing Authorisation Number HR-H-320070484
Active Substance lenalidomid
Composition jedna kapsula sadrži 10 mg lenalidomida
Pharmaceutical Form kapsula, tvrda
Packaging [MA Number for Packaging] 21 kapsula u blisteru, u kutiji  [HR-H-320070484-01]
21 kapsula u blisteru s jediničnom dozom, u kutiji  [HR-H-320070484-02]
7 kapsula u blisteru, u kutiji  [HR-H-320070484-03]
Manufacturer Pharmadox Healthcare Limited, Paola PLA, Malta
Aristo Pharma GmbH, Berlin, Njemačka
Marketing Authorisation Holder Aristo Pharma GmbH, Wallenroder Strasse 8-10, Berlin, Njemačka
Marketing Authorisation Date 09.09.2020
MA Period of Validity 09.09.2025
MA Revocation Date 11.01.2023*
Classification Number UP/I-530-09/19-01/92
Registration Number 381-12-01/70-20-03
Prescription na recept
Type of prescription ograničeni recept
Distribution u ljekarni
Advertising to general public zabranjeno
ATC Code L04AX04
Medicinal product marketed in the Croatia Trajni prekid opskrbe
SmPC download
PL download
Public Assessment Report download
Summary of risk management plan 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Marketing authorisation has been revoked by request of the marketing authorisation holder.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.

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