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PRODUCT DETAIL

Alunbrig 90 mg filmom obalené tablety

Code 9787C
MA number EU/1/18/1264/007
Product Form: tbl flm 7x90 mg (blis.Aclar/Al)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Takeda Pharma A/S, Denmark
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01E Protein kinase inhibitors
L01ED Anaplastic lymphoma kinase (ALK) inhibitors
L01ED04 Brigatinib
Shelf life: 36
Route of admin.: Oral use
Prescription Status: Medicinal product subject to restricted medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 22.11.2018
SmPC + PL: European Medicines Agency's database
Dokument: Alunbrig_Karta pacienta.pdf  
Safety feature Yes
Data update: 18.08.2023
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