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PRODUCT DETAIL

Rapilysin 10 U prášok a rozpúšťadlo na injekčný roztok

Code 28692
MA number EU/1/96/018/001
Product Form: plv iol 2x10 U+2x10 ml solv. (liek.inj.skl.+striek.skl.napln.+2 bodce na rekonštitúciu+2 inj.ihly 19 G1)
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
B01AD Enzymes
B01AD07 Reteplase
Shelf life: 36
Container: glass container
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application
MA issued: 29.08.1996
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 19.06.2018
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