Bortezomib Hospira

Medicinal product

(Invented) name

Bortezomib Hospira

Active substance (s)

Bortezomibas

Strength

3,5 mg

Pharmaceutical form

milteliai injekciniam tirpalui

Route (s) of administration

leisti į veną, leisti po oda

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

L01XG01, bortezomib

Marketing authorisation holder

Pfizer Europe MA EEIG, Belgija

Date of authorisation

2016-07-22

Date of renewal

Documents

Search in EMA Europe

Stage

Išregistruotas

Controlled?

No

Controlled substance type

Legal basis

10(1)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Powder for solution for injection	1 vnt.
Bortezomibas	3,5 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
66261	80784	1080784	flakonas	N1		Receptinis	EU/1/16/1114/001	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2025-08-08	Išregistruotas
2016-07-22	Registruotas