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EMA Product

Ranexa (previously Latixa)

Product approved by European Medicines Agency (EU)

Basic Information

Ranexa (previously Latixa)

Regulatory Information

EMEA/H/C/000805

Authorised

July 8, 2008

23

April 10, 2024

Company Information

Luxembourg

Menarini International Operations Luxembourg S.A. 1, Avenue de la Gare L-1611 Luxembourg

MENARINI INTERNATIONAL OPERATIONS LUXEMBOURG S.A.

Active Substances Detail

Detailed Information

Therapeutic Indication

### Therapeutic indication Ranexa is indicated as add-on therapy for the symptomatic treatment of patients with stable angina pectoris who are inadequately controlled or intolerant to first-line anti-anginal therapies (such as beta-blockers and / or calcium antagonists).

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

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