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PRODUCT DETAIL

Kapruvia 50 mikrogramov/ml injekčný roztok

Code 0660E
MA number EU/1/22/1643/002
Product Form: sol inj 12x1 ml/50 µg (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 87 - VARIA I
ATC:
V VARIOUS
V03 ALL OTHER THERAPEUTIC PRODUCTS
V03A ALL OTHER THERAPEUTIC PRODUCTS
V03AX Other therapeutic products
V03AX04 Difelikefalin
Shelf life: 24
Container: glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 25.04.2022
Validity: 25.04.2027
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 09.05.2022
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