Rapilysin

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Withdrawn

This medicine's authorisation has been withdrawn

reteplase
MedicineHumanWithdrawn

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  • Application under evaluation
  • CHMP opinion
  • European Commission decision

Overview

On 26 January 2024, the European Commission withdrew the marketing authorisation for Rapilysin (reteplase) in the European Union (EU). The withdrawal was at the request of the marketing authorisation holder, Actavis Group PTC ehf., which notified the European Commission of its decision to permanently discontinue the marketing of the product for commercial reasons.

Rapilysin was granted marketing authorisation in the EU on 29 August 1996 for the treatment of suspected myocardial infarction. The marketing authorisation was initially valid for a 5-year period. It was subsequently renewed for an additional 5-year period in 2001. It was then granted unlimited validity in 2006. 

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Product information

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Latest procedure affecting product information:IG1612
31/05/2023
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This medicine’s product information is available in all official EU languages.
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Product information documents contain:

  • summary of product characteristics (annex I);
  • manufacturing authorisation holder responsible for batch release (annex IIA);
  • conditions of the marketing authorisation (annex IIB);
  • labelling (annex IIIA);
  • package leaflet (annex IIIB).

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Product details

Name of medicine
Rapilysin
Active substance
reteplase
International non-proprietary name (INN) or common name
reteplase
Therapeutic area (MeSH)
Myocardial Infarction
Anatomical therapeutic chemical (ATC) code
B01AD07

Pharmacotherapeutic group

Antithrombotic agents

Therapeutic indication

Rapilysin is indicated for the thrombolytic treatment of suspected myocardial infarction with persistent ST elevation or recent left bundle branch block within 12 hours after the onset of acute-myocardial-infarction (AMI) symptoms.

Authorisation details

EMA product number
EMEA/H/C/000105
Marketing authorisation holder
Actavis Group PTC ehf

Dalshraun 1
220 Hafnarfjörður
Iceland

Marketing authorisation issued
29/08/1996
Withdrawal of marketing authorisation
26/01/2024
Revision
28

Assessment history

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