Lenalidomide Krka d.d. Novo mesto
The medicinal product has been authorised by the European Commission (EC) via centralised procedure in all EU Member States, based on the European Medicines Agency (EMA) experts' opinion.
| Name | Lenalidomide Krka d.d. Novo mesto |
|---|---|
| Former Name | Lenalidomide Krka |
| Active Substance | lenalidomidklorid hidrat |
| Prescription | na recept |
| Type of prescription | ograničeni recept |
| Distribution | u ljekarni |
| ATC Code | L04AX04 |
| Summary of product characteristics (SmPC), labelling and package leaflet (PL) | download |
| Link to the European Medicines Agency's (EMA) product information | download |
| Link to the European Commission's (EC) decisions | download |
