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PRODUCT DETAIL

Rozlytrek 50 mg filmom obalený granulát vo vrecúšku

Code 7009E
MA number EU/1/20/1460/003
Product Form: gra flm 42x50 mg (vre.PET/Al/PE)
MA Status: Ex - Conditional centralised marketing authorisation
Type of procedure: EU
MAH, country: Roche Registration GmbH, Germany
Therapeutic Class: 44 - CYTOSTATICA
ATC:
L ANTINEOPLASTIC AND IMMUNOMODULATING AGENTS
L01 ANTINEOPLASTIC AGENTS
L01E Protein kinase inhibitors
L01EX Other protein kinase inhibitors
L01EX14 Entrectinib
Shelf life: 24
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: 31.07.2020
Validity: 03.08.2025
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 06.08.2024
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