DuoCover: Withdrawal of the marketing authorisation application

Overview

On 23 May 2008, Bristol Myers Squibb Pharma EEIG officially notified the Committee for Medicinal Products for Human Use (CHMP) that it wishes to withdraw its application for a marketing authorisation for DuoCover for the prevention of atherothrombotic events.

  • List item

    Questions and answers on the withdrawal of the marketing application for DuoCover (PDF/56.94 KB)


    First published: 09/06/2008
    Last updated: 31/03/2010
    EMEA/270168/2008

  • Key facts

    Name
    DuoCover
    Product number
    EMEA/H/C/000875
    Active substance
    • clopidogrel
    • Acetylsalicylic acid
    Date of withdrawal
    23/05/2008
    Company making the application
    Bristol Myers Squibb Pharma EEIG
    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.

    An assessment report is published when the application is withdrawn after the first stage of the CHMP's evaluation is completed ('day 120').

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