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Irish Medicines Database · HPRA register

Adjupanrix suspension and emulsion for emulsion for injection. Pandemic influenza vaccine (H5N1) (split virion, inactivated, adjuvanted)

Authorisation EU/1/09/578/001 · GlaxoSmithKline Biologicals S.A.

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Adjupanrix suspension and emulsion for emulsion for injection. Pandemic influenza vaccine (H5N1) (split virion, inactivated, adjuvanted)
Licence EU/1/09/578/001 · Unknown
Licence holder
GlaxoSmithKline Biologicals S.A. (all products →)
Active substance
Purified antigen fractions of inactivated split virions a/vietnam/1194/2004 nibrg-14 (h5n1)
Dosage form
Emulsion and suspension for emulsion for injection
Route of administration
Intramuscular use
ATC codes
J07BB, J07BB02
First authorised
05/11/2009
Prescription status
Product subject to prescription which may not be renewed (A)
Supply
Supply through pharmacies only
Legal basis
Full application (Article 8(3) of Directive No 2001/83/EC)

Data: Health Products Regulatory Authority (HPRA) open dataset, licensed CC BY 4.0, published 04 Jul 2026. This listing is regulatory information, not medical advice — consult the package leaflet, SPC, or a healthcare professional. For the authoritative record see the HPRA register.