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PRODUCT DETAIL

Eliquis 0,15 mg granulát v kapsulách na otváranie

Code 7579E
MA number EU/1/11/691/016
Product Form: gra cps 28x0,15 mg (fľ.HDPE)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Bristol-Myers Squibb/Pfizer EEIG , Ireland
Therapeutic Class: 16 - ANTICOAGULANTIA (FIBRINOLYTICA, ANTIFIBRINOL.)
ATC:
B BLOOD AND BLOOD FORMING ORGANS
B01 ANTITHROMBOTIC AGENTS
B01A ANTITHROMBOTIC AGENTS
B01AF Direct factor Xa inhibitors
B01AF02 Apixaban
Shelf life: 36
Route of admin.: Oral use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 18.05.2011
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 20.09.2024
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