🇺🇸 tirofiban high-bolus dose regimen in United States

FDA authorised tirofiban high-bolus dose regimen on 14 May 1998

Marketing authorisations

FDA — authorised 14 May 1998

  • Application: NDA020912
  • Marketing authorisation holder: MEDICURE
  • Local brand name: AGGRASTAT
  • Indication: INJECTABLE — INJECTION
  • Status: approved

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FDA — authorised 14 May 1998

  • Application: NDA020913
  • Marketing authorisation holder: MEDICURE
  • Local brand name: AGGRASTAT
  • Indication: SOLUTION — INTRAVENOUS
  • Status: approved

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FDA

  • Status: approved

tirofiban high-bolus dose regimen in other countries

Same drug, different regulators. Each page below lists the local marketing authorisation, HTA position, pricing, and adverse-event data.

Frequently asked questions

Is tirofiban high-bolus dose regimen approved in United States?

Yes. FDA authorised it on 14 May 1998; FDA authorised it on 14 May 1998; FDA has authorised it.

Who is the marketing authorisation holder for tirofiban high-bolus dose regimen in United States?

MEDICURE holds the US marketing authorisation.