Aerinaze

RSS

desloratadine / pseudoephedrine

Authorised
This medicine is authorised for use in the European Union.

Overview

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

This EPAR was last updated on 12/05/2021

Authorisation details

Product details
Name
Aerinaze
Agency product number
EMEA/H/C/000772
Active substance
  • desloratadine
  • pseudophedrine sulfate
International non-proprietary name (INN) or common name
  • desloratadine
  • pseudoephedrine
Therapeutic area (MeSH)
Rhinitis, Allergic, Seasonal
Anatomical therapeutic chemical (ATC) code
R01BA52
Publication details
Marketing-authorisation holder
N.V. Organon
Revision
19
Date of issue of marketing authorisation valid throughout the European Union
30/07/2007
Contact address

Kloosterstraat 6
5349 AB, Oss
Netherlands

Product information

13/04/2021 Aerinaze - EMEA/H/C/000772 - T/0043

Contents

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

Pharmacotherapeutic group

Nasal preparations

Therapeutic indication

Symptomatic treatment of seasonal allergic rhinitis when accompanied by nasal congestion.

Assessment history

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