Pantecta Control

RSS

pantoprazole

Withdrawn
This medicine is now withdrawn from use in the European Union.

Overview

The marketing authorisation for Pantecta Control has been withdrawn at the request of the marketing-authorisation holder.

This EPAR was last updated on 15/11/2016

Authorisation details

Product details
Name
Pantecta Control
Agency product number
EMEA/H/C/001099
Active substance
pantoprazole
International non-proprietary name (INN) or common name
pantoprazole
Therapeutic area (MeSH)
Gastroesophageal Reflux
Anatomical therapeutic chemical (ATC) code
A02BC02
Publication details
Marketing-authorisation holder
Takeda GmbH
Revision
7
Date of issue of marketing authorisation valid throughout the European Union
12/06/2009
Contact address
Byk-Gulden-Strasse 2
D-78467 Konstanz
Germany

Product information

19/09/2016 Pantecta Control - EMEA/H/C/001099 - IG/0634

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

Please note that the size of the above document can exceed 50 pages.

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

Pharmacotherapeutic group

Proton pump inhibitors

Therapeutic indication

Short-term treatment of reflux symptoms (e.g. heartburn, acid regurgitation) in adults.

Assessment history

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