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Irish Medicines Database · HPRA register

Cervarix suspension for injection Human Papillomavirus vaccine [Types 16, 18] (Recombinant, adjuvanted, adsorbed)

Authorisation EU/1/07/419/1-12 · GlaxoSmithKline Biologicals S.A.

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Cervarix suspension for injection Human Papillomavirus vaccine [Types 16, 18] (Recombinant, adjuvanted, adsorbed)
Licence EU/1/07/419/1-12 · Unknown
Licence holder
GlaxoSmithKline Biologicals S.A. (all products →)
Active substances
Hpv 16 l1 protein, Hpv 18 l1 protein
Dosage form
Suspension for injection
Route of administration
Intramuscular use
ATC codes
J07BM, J07BM02
First authorised
20/09/2007
Prescription status
Product subject to prescription which may not be renewed (A)
Supply
Supply through pharmacies only
Legal basis
New active substance (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.