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PRODUCT DETAIL

INTEGRILIN 0,75 mg/ml infúzny roztok

Code 46802
MA number EU/1/99/109/001
Product Form: sol inf 1x100 ml/75 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
B01AC16 Eptifibatide
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
MA issued: 01.07.1999
SmPC + PL: European Medicines Agency's database
Dokument: DHPC_Integrilin_02.11.2023.pdf  
Safety feature Yes
Data update: 08.12.2021
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