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EMA Product

Vaniqa

Product approved by European Medicines Agency (EU)

Basic Information

Vaniqa

Regulatory Information

EMEA/H/C/000325

Authorised

March 19, 2001

24

November 27, 2024

Company Information

Spain

Ronda General Mitre, 151 ES-08022 Barcelona

Almirall, LLC

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Treatment of facial hirsutism in women.

Overview Summary

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

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