Pioglitazone ratio: Withdrawal of the marketing authorisation application
pioglitazone
Table of contents
Overview
On 3 February 2012, ratiopharm GmbH officially notified the Committee for Medicinal Products for Human Use (CHMP) that it wishes to withdraw its application for a marketing authorisation for Pioglitazone ratio, for the treatment of type 2 diabetes.
Key facts
Name |
Pioglitazone ratio |
Product number |
EMEA/H/C/002370 |
International non-proprietary name (INN) or common name |
|
Active substance |
|
Date of withdrawal |
03/02/2012 |
Withdrawal type |
Initial authorisation |
All documents
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Withdrawal assessment report for Pioglitazone Ratio (PDF/307.88 KB)
First published: 12/07/2012
Last updated: 12/07/2012
EMA/391408/2012 -
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Withdrawal letter: Pioglitazone ratio (PDF/80.16 KB)
First published: 30/04/2012
Last updated: 30/04/2012 -
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Questions and answers on the withdrawal of the marketing authorisation application for Pioglitazone ratio (PDF/55.27 KB)
First published: 30/04/2012
Last updated: 12/07/2012
EMA/281366/2012 -
Related information on withdrawals
A question-and-answer (Q&A) document provides a summary of the CHMP's evaluation of the medicine at the time of the withdrawal of the application, and includes a link to the company's formal withdrawal letter.
An assessment report is published when the application is withdrawn after the first stage of the CHMP's evaluation is completed ('day 120').