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PRODUCT DETAIL

Inhixa 8 000 IU (80 mg/ml)/0,8 ml injekčný roztok

Code 5920C
MA number EU/1/16/1132/029
Product Form: sol inj 12x0,8 ml/80 mg (striek.inj.napl.skl. s krytom ihly)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Techdow Pharma Netherlands B.V., Netherland
Therapeutic Class: 16 - ANTICOAGULANTIA (FIBRINOLYTICA, ANTIFIBRINOL.)
ATC:
B BLOOD AND BLOOD FORMING ORGANS
B01 ANTITHROMBOTIC AGENTS
B01A ANTITHROMBOTIC AGENTS
B01AB Heparin group
B01AB05 Enoxaparin
Shelf life: 36
Container: pre-filled syringe
Route of admin.: Extracorporeal, intravenous and subcutaneous use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 10(4) similar biological application
MA issued: 27.10.2017
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 07.09.2021
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