Pioglitazone ratiopharm: Withdrawal of the marketing authorisation application

pioglitazone

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 ratiopharm, for the treatment of type 2 diabetes.

  • List item

    Questions and answers on the withdrawal of the marketing authorisation application for Pioglitazone ratiopharm (PDF/55.52 KB)


    First published: 30/04/2012
    Last updated: 12/07/2012
    EMA/281372/2012

  • Key facts

    Name
    Pioglitazone ratiopharm
    Product number
    EMEA/H/C/002260
    International non-proprietary name (INN) or common name
    • pioglitazone
    Active substance
    • pioglitazone
    Date of withdrawal
    03/02/2012
    Withdrawal type
    Initial authorisation

    All documents

    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 (withdrawal letter Doc. type, leave the 'Author' in properties blank).

    An assessment report is published when the application is withdrawn after the first stage of the CHMP's evaluation is completed ('day 120').

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