Table of contents
This is a summary of the European public assessment report (EPAR) for Neoclarityn. 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 Neoclarityn.
Neoclarityn : EPAR - Summary for the public (PDF/75.37 KB)
First published: 13/08/2008
Last updated: 30/06/2015
Neoclarityn : EPAR - Risk-management-plan summary (PDF/1.86 MB)
First published: 22/06/2021
|Agency product number||
|International non-proprietary name (INN) or common name||
|Therapeutic area (MeSH)||
|Anatomical therapeutic chemical (ATC) code||
|Date of issue of marketing authorisation valid throughout the European Union||
14/12/2022 Neoclarityn - EMEA/H/C/000314 - IG1573
This medicine’s product information is available in all official EU languages.
Select ‘available languages’ to access the language you need.
Product information documents contain:
- summary of product characteristics (annex I);
- manufacturing authorisation holder responsible for batch release (annex IIA);
- conditions of the marketing authorisation (annex IIB);
- labelling (annex IIIA);
- package leaflet (annex IIIB).
You can find product information documents for centrally authorised human medicines on this website. For centrally authorised veterinary medicines authorised or updated from February 2022, see the Veterinary Medicines Information website.
Antihistamines for systemic use
Neoclarityn is indicated for the relief of symptoms associated with:
- allergic rhinitis