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PRODUCT DETAIL

BIMERVAX LP.8.1 injekčná emulzia

Code 1711F
MA number EU/1/22/1709/010
Product Form: emu inj 20x0,5 ml (liek.inj.skl.jednodávk.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Hipra Human Health, S.L.U., Spain
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
J ANTIINFECTIVES FOR SYSTEMIC USE
J07 VACCINES
J07B VIRAL VACCINES
J07BN Covid-19 vaccines
J07BN04 Covid-19, protein subunit
Shelf life: 12
Container: multidose glass vial
Route of admin.: Intravenous use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 30.03.2023
Validity: 30.03.2028
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 20.10.2025
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