en

PRODUCT DETAIL

Rozlytrek 200 mg tvrdé kapsuly

Code 5483D
MA number EU/1/20/1460/002
Product Form: cps dur 90x200 mg (fľ.HDPE)
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: 48
Container: bottle HDPE
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: 10.06.2024
eu-flag.png sk-flag.png