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EMA Product

Sildenafil ratiopharm

Product approved by European Medicines Agency (EU)

Basic Information

Sildenafil ratiopharm

Regulatory Information

EMEA/H/C/001080

Authorised

December 23, 2009

19

June 24, 2022

Company Information

Germany

Graf-Arco-Str. 3 D-89079 Ulm

ratiopharm GmbH

Drug Classification

Generic Medicine

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of men with erectile dysfunction, which is the inability to achieve or maintain a penile erection sufficient for satisfactory sexual performance. In order for sildenafil to be effective, sexual stimulation is required.

Overview Summary

This is a summary of the European public assessment report (EPAR) for sildenafil. 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 sildenafil.

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