Somavert

Medicinal product

(Invented) name

Somavert

Active substance (s)

Pegvizomantas

Strength

20 mg

Pharmaceutical form

milteliai ir tirpiklis injekciniam tirpalui

Route (s) of administration

leisti po oda

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

No

ATC code (s)

H01AX01, Pegvisomant

Marketing authorisation holder

Pfizer Europe MA EEIG, Belgija

Date of authorisation

2002-11-13

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 and solvent for solution for injection	1 vnt.
Pegvizomantas	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
28286	30816	1030816	flakonas	ir užpildytas švirkštas N30		Receptinis	EU/1/02/240/003	Netiekiama	-	-	No	-	-
28287	30817	1030817	flakonas	ir užpildytas švirkštas N1		Receptinis	EU/1/02/240/004	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2002-11-13	Registruotas