IDflu
influenza vaccine (split virion, inactivated)
Table of contents
Withdrawn
This medicine is now withdrawn from use in the European Union.
Overview
The marketing authorisation for IDflu has been withdrawn at the request of the marketing authorisation holder.
This EPAR was last updated on 29/03/2018
Authorisation details
| Product details | |
|---|---|
| Name |
IDflu
|
| Agency product number |
EMEA/H/C/000966
|
| Active substance |
influenza virus (inactivated, split) of the following strains:A/California/7/2009 (H1N1)pdm09 - like strain (A/California/7/2009, NYMC X-179A)A/Hong Kong/4801/2014 (H3N2) - like strain (A/Hong Kong/4801/2014, NYMC X-263B)B/Brisbane/60/2008 - like strain (B/Brisbane/60/2008, wild type)
|
| International non-proprietary name (INN) or common name |
influenza vaccine (split virion, inactivated)
|
| Therapeutic area (MeSH) |
|
| Anatomical therapeutic chemical (ATC) code |
J07BB02
|
| Publication details | |
|---|---|
| Marketing-authorisation holder |
Sanofi Pasteur S.A.
|
| Revision |
13
|
| Date of issue of marketing authorisation valid throughout the European Union |
24/02/2009
|
| Contact address | |
Product information
03/01/2017 IDflu - EMEA/H/C/000966 - N/0048
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
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You are therefore advised to be selective about which sections or pages you wish to print.
Pharmacotherapeutic group
Pharmacotherapeutic group
Vaccines
Therapeutic indication
Therapeutic indication
Prophylaxis of influenza in individuals 60 years of age and over, especially in those who run an increased risk of associated complications.
The use of IDflu should be based on official recommendations.