Ruxolitinib Viatris

Medicinal product

(Invented) name

Ruxolitinib Viatris

Active substance (s)

Ruksolitinibas

Strength

20 mg

Pharmaceutical form

tabletės

Route (s) of administration

vartoti per burną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

L01EJ01, ruxolitinib

Marketing authorisation holder

Viatris Limited, Airija

Date of authorisation

2026-09-18

Date of renewal

Documents

Search in EMA Europe

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

10(1)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Tabletėje yra:	1 vnt.
Ruksolitinibas	20 mg

Packages

PAKID	NPAKID	NPAKID-7	Pack type	Pack size	Type of packaging	Proposed dispensing/classification	Marketing authorisation no.	Supply status	From	To	Package is in foreign language	From	To	Mock-up
122433	108545	1108545	lizdinė plokštelė	N56		Receptinis	EU/1/26/2064/010	Netiekiama	-	-	No	-	-
122434	108546	1108546	lizdinė plokštelė	N56 (kalendorinė)	kalendorinė pakuotė	Receptinis	EU/1/26/2064/011	Netiekiama	-	-	No	-	-
122435	108547	1108547	dalomoji lizdinė plokštelė	N56×1		Receptinis	EU/1/26/2064/012	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2026-09-18	Registruotas