Urorec

RSS

silodosin

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

Overview

This is a summary of the European public assessment report (EPAR). It explains how the Committee for Medicinal Products for Human Use (CHMP) assessed the studies performed, to reach its recommendations on how to use the medicine.

If you need more information about your medical condition or your treatment, read the package leaflet (also part of the EPAR) or contact your doctor or pharmacist. If you want more information on the basis for the CHMP recommendations, read the scientific discussion (also part of the EPAR).

This EPAR was last updated on 06/04/2022

Authorisation details

Product details
Name
Urorec
Agency product number
EMEA/H/C/001092
Active substance
silodosin
International non-proprietary name (INN) or common name
silodosin
Therapeutic area (MeSH)
Prostatic Hyperplasia
Anatomical therapeutic chemical (ATC) code
G04CA04
Publication details
Marketing-authorisation holder
Recordati Ireland Ltd
Revision
18
Date of issue of marketing authorisation valid throughout the European Union
29/01/2010
Contact address

Raheens East
Ringaskiddy
Co. Cork
Ireland

Product information

04/04/2022 Urorec - EMEA/H/C/001092 - N/0052

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Product information documents contain:

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.

Pharmacotherapeutic group

Urologicals

Therapeutic indication

Treatment of the signs and symptoms of benign prostatic hyperplasia (BPH).

Assessment history

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