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PRODUCT DETAIL

ReFacto AF 1000 IU, prášok a rozpúšťadlo na injekčný roztok

Code 13141
MA number EU/1/99/103/003
Product Form: plv iol 1x1000 IU+1x4 ml solv.(liek.inj.skl.+striek.inj.skl.napl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 16 - ANTICOAGULANTIA (FIBRINOLYTICA, ANTIFIBRINOL.)
ATC:
B BLOOD AND BLOOD FORMING ORGANS
B02 ANTIHEMORRHAGICS
B02B LOCAL HEMOSTATICS, COMBINATIONS
B02BD Blood coagulation factors
B02BD02 Coagulation factor VIII
Shelf life: 36
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application
MA issued: 13.04.1999
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 19.06.2018
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