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Novartis receives European marketing authorization for Aclasta® - News


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Novartis receives European marketing authorization for Aclasta®

Sat, 23 Apr 2005 07:00 PM EST

... Novartis Pharma AG announced today that Aclasta® (zoledronic acid 5mg solution for infusion) has been granted Marketing Authorization by the European Commission for the treatment of Paget's disease of the bone in all 25 European member states, as well as Norway and Iceland... click link for more info. ...

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