Neulasta

Medicinal product

(Invented) name

Neulasta

Active substance (s)

Pegfilgrastimas

Strength

6 mg

Pharmaceutical form

injekcinis tirpalas

Route (s) of administration

leisti po oda

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

L03AA13, Pegfilgrastim

Marketing authorisation holder

Amgen Europe B.V., Nyderlandai

Date of authorisation

2002-08-22

Date of renewal

Documents

Search in EMA Europe

Stage

Išregistruotas

Controlled?

No

Controlled substance type

Legal basis

8(3)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

solution for injection	0.6 ml
Pegfilgrastimas	6 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
26909	29473	1029473	užpildytas švirkštiklis	0,6 ml N1 SureClick		Receptinis	EU/1/02/227/003	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
	Išregistruotas
2002-08-22	Registruotas