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PRODUCT DETAIL

Ruconest 2100 U, prášok a rozpúšťadlo na injekčný roztok

Code 2630C
MA number EU/1/10/641/002
Product Form: plv iol 1x2100 U + 20 ml solv. (liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
Therapeutic Class: 87 - VARIA I
ATC:
B BLOOD AND BLOOD FORMING ORGANS
B06 OTHER HEMATOLOGICAL AGENTS
B06A OTHER HEMATOLOGICAL AGENTS
B06AC Drugs used in hereditary angioedema
B06AC04 Conestat alfa
Shelf life: 48
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: 28.10.2010
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 12.05.2020
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