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PRODUCT DETAIL

Uptravi 200 mikrogramov filmom obalené tablety

Code 9490B
MA number EU/1/15/1083/001
Product Form: tbl flm 10x200 µg (blis.PA/Al/HDPE/PE/Al)
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
B01AC27 Selexipag
Shelf life: 36
Container: blister PA/Al/HDPE/PE/Al
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 12.05.2016
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 04.01.2022
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