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PRODUCT DETAIL

Kengrexal 50 mg prášok na injekčný/infúzny koncentrát

Code 4209B
MA number EU/1/15/994/001
Product Form: plc ifu 10x50 mg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 16 - ANTICOAGULANTIA (FIBRINOLYTICA, ANTIFIBRINOL.)
ATC:
B BLOOD AND BLOOD FORMING ORGANS
B01 ANTITHROMBOTIC AGENTS
B01A ANTITHROMBOTIC AGENTS
B01AC Platelet aggregation inhibitors excl. heparin
B01AC25 Cangrelor
Shelf life: 36
Container: glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 23.03.2015
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 26.06.2023
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