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PRODUCT DETAIL

Arixtra 5 mg/0,4 ml injekčný roztok, naplnená injekčná striekačka

Code 97425
MA number EU/1/02/206/018
Product Form: sol inj 20x0,4 ml/5 mg (striek.inj.napl.skl. s autom.zabezp.syst.)
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
B01AX Other antithrombotic agents
B01AX05 Fondaparinux
Shelf life: 36
Container: glass pre-filled syringe
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - known active substance
MA issued: 21.03.2002
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 19.02.2021
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