Prepandrix

Medicinal product

(Invented) name

Prepandrix

Active substance (s)

A/Indonesia/05/2005 (H5N1) panaši padermė, panaudojus (PR8-IBCDC-RG2)

Strength

3,75 µg/dozėje

Pharmaceutical form

suspensija ir emulsija injekcinei emulsijai

Route (s) of administration

leisti į raumenis

Legal status for supply

Receptinis

Narrow therapeutic index (NTI)

ATC code (s)

J07BB02, influenza, inactivated, split virus or surface antigen

Marketing authorisation holder

GlaxoSmithKline Biologicals s.a., Belgija

Date of authorisation

2008-05-14

Date of renewal

Documents

Stage

Išregistruotas

Controlled?

Controlled substance type

Legal basis

8(3)

Procedure number

Marketing authorisation procedure

Centrinė registracija

Qualitative and quantitative composition

Suspension and Emulsion for emulsion for injection	0.5 ml
A/Indonesia/05/2005 (H5N1) panaši padermė, panaudojus (PR8-IBCDC-RG2)	3,75 µg

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
37226	50846	1050846	flakonas	N50 (suspensija) + N2 x 25 (emulsija)		Receptinis	EU/1/08/453/002	Netiekiama	-	-	No	-	-

Stadijos

Data	Stadija
2021-01-04	Išregistruotas
2008-05-14	Registruotas