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EMA Product

Emadine

Product approved by European Medicines Agency (EU)

Basic Information

Emadine

Regulatory Information

EMEA/H/C/000223

Authorised

January 27, 1999

28

July 10, 2022

Company Information

Sweden

Solnavagen 3H 113 63 Stockholm

Immedica Pharma Ab

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Symptomatic treatment of seasonal allergic conjunctivitis.

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 their 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 of the CHMP recommendations, read the scientific discussion (also part of the EPAR).

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