Table of contents
The marketing authorisation for Ipreziv has been withdrawn at the request of the marketing authorisation holder.
Ipreziv : EPAR - Summary for the public (PDF/520.34 KB)
First published: 15/12/2011
Last updated: 19/12/2014
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|International non-proprietary name (INN) or common name||
|Therapeutic area (MeSH)||
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This medicine is under additional monitoring, meaning that it is monitored even more intensively than other medicines. For more information, see Medicines under additional monitoring.
Takeda Pharma A/S
|Date of issue of marketing authorisation valid throughout the European Union||
Dybendal Alle 10
27/10/2014 Ipreziv - EMEA/H/C/002517 - A31/0006
This medicine’s product information is available in all official EU languages.
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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.
Agents acting on the renin-angiotensin system
Ipreziv is indicated for the treatment of essential hypertension in adults.