🇪🇺 integrilin in European Union

EMA authorised integrilin on 1 July 1999

Marketing authorisation

EMA — authorised 1 July 1999

  • Application: EMEA/H/C/000230
  • Marketing authorisation holder: GlaxoSmithKline Trading Services Limited
  • Local brand name: Integrilin
  • Indication: Integrilin is intended for use with acetylsalicylic acid and unfractionated heparin. Integrilin is indicated for the prevention of early myocardial infarction in patients presenting with unstable angina or non-Q-wave myocardial infarction with the last episode of chest pain occurring within 24 hours and with ECG changes and / or elevated cardiac enzymes. Patients most likely to benefit from Integrilin treatment are those at high risk of developing myocardial infarction within the first 3-4 days after onset of acute angina symptoms including for instance those that are likely to undergo an earl
  • Status: withdrawn

Read official source →

Other Cardiovascular approved in European Union

Frequently asked questions

Is integrilin approved in European Union?

Yes. EMA authorised it on 1 July 1999.

Who is the marketing authorisation holder for integrilin in European Union?

GlaxoSmithKline Trading Services Limited holds the EU marketing authorisation.