Kyprolis

Medicinal product

(Invented) name

Kyprolis

Active substance (s)

Karfilzomibas

Strength

30 mg

Pharmaceutical form

milteliai infuziniam tirpalui

Route (s) of administration

leisti į veną

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

L01XG02, carfilzomib

Marketing authorisation holder

Amgen Europe B.V., Nyderlandai

Date of authorisation

2015-11-19

Date of renewal

Documents

Search in EMA Europe

Stage

Registruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Powder for solution for infusion	1 vnt.
Karfilzomibas	30 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
67806	82363	1082363	flakonas	N1		Receptinis	EU/1/15/1060/003	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2015-11-19	Registruotas