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EMA Product

Sildenafil Teva

Product approved by European Medicines Agency (EU)

Basic Information

Sildenafil Teva

Regulatory Information

EMEA/H/C/001073

Authorised

November 30, 2009

September 24, 2009

17

July 4, 2022

Company Information

the netherlands

Teva B.V. Swensweg 5 2031 GA Haarlem

Teva Pharma B.V.

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 Teva to be effective, sexual stimulation is required.

Overview Summary

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

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