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EMA Product

Silodyx

Product approved by European Medicines Agency (EU)

Basic Information

Silodyx

Regulatory Information

EMEA/H/C/001209

Authorised

January 29, 2010

17

March 14, 2025

Company Information

Ireland

Raheens East Ringaskiddy Co. Cork

Recordati Ireland Ltd.

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of the signs and symptoms of benign prostatic hyperplasia (BPH)

Overview Summary

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach its recommendations on how to use the medicine. If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis for the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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