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Irish Medicines Database · HPRA register

BIMERVAX emulsion for injection COVID-19 Vaccine (recombinant, adjuvanted)

Authorisation EU/1/22/1709/001-004 · Hipra Human Health S.L.

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BIMERVAX emulsion for injection COVID-19 Vaccine (recombinant, adjuvanted)
Licence EU/1/22/1709/001-004 · Unknown
Licence holder
Hipra Human Health S.L. (all products →)
Active substance
SARS-CoV-2 virus, variants B.1.351-B.1.1.7, spike protein, receptor binding domain fusion heterodimer
Dosage form
Emulsion for injection
Route of administration
Intramuscular use
ATC code
J07BN01
First authorised
30/03/2023
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.