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PRODUCT DETAIL

ANDEMBRY 200 mg injekčný roztok v naplnenom pere

Code 9116E
MA number EU/1/24/1885/003
Product Form: sol inj 1x1,2 ml/200 mg (pero napl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: CSL Behring GmbH, Germany
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
B06AC07 Garadacimab
Shelf life: 36
Route of admin.: Subcutaneous use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 10.02.2025
Validity: 10.02.2030
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 03.03.2025
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