Alisade

RSS

fluticasone furoate

Withdrawn
This medicine is now withdrawn from use in the European Union.

Overview

The marketing authorisation for Alisade has lapsed because it has not been marketed in the European Union in the three years following the granting of the authorisation.

This EPAR was last updated on 18/10/2011

Authorisation details

Product details
Name
Alisade
Agency product number
EMEA/H/C/001019
Active substance
fluticasone furoate
International non-proprietary name (INN) or common name
fluticasone furoate
Therapeutic area (MeSH)
  • Rhinitis, Allergic, Perennial
  • Rhinitis, Allergic, Seasonal
Anatomical therapeutic chemical (ATC) code
R01AD12
Publication details
Marketing-authorisation holder
Glaxo Group Ltd.
Revision
4
Date of issue of marketing authorisation valid throughout the European Union
06/10/2008
Contact address
Glaxo Group Limited
Greenford Road
Greenford, Middx UB6 0NN
United Kingdom

Product information

17/02/2010 Alisade - EMEA/H/C/001019 - IB/0007

Contents

  • Annex I - Summary of product characteristics
  • Annex IIA - Manufacturing-authorisation holder responsible for batch release
  • Annex IIB - Conditions of the marketing authorisation
  • Annex IIIA - Labelling
  • Annex IIIB - Package leaflet

Please note that the size of the above document can exceed 50 pages.

You are therefore advised to be selective about which sections or pages you wish to print.

Pharmacotherapeutic group

NASAL PREPARATIONS

Therapeutic indication

Adults, adolescents (12 years and over) and children (6 - 11 years). Alisade is indicated for the treatment of the symptoms of allergic rhinitis.

Assessment history

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