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EMA Product

Myclausen

Product approved by European Medicines Agency (EU)

Basic Information

Myclausen

Regulatory Information

EMEA/H/C/001218

Authorised

October 7, 2010

16

April 11, 2024

Company Information

Germany

Eiderstedter Weg 3 14129 Berlin

Passauer Pharma GmbH

Drug Classification

Generic Medicine

Active Ingredients

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Myclausen is indicated in combination with ciclosporin and corticosteroids for the prophylaxis of acute transplant rejection in patients receiving allogeneic renal, cardiac or hepatic transplants.

Overview Summary

This is a summary of the European public assessment report (EPAR) for Myclausen. It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the medicine to reach its opinion in favour of granting a marketing authorisation and its recommendations on the conditions of use for Myclausen.

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