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PRODUCT DETAIL

Abrysvo prášok a rozpúšťadlo na injekčný roztok

Code 7540E
MA number EU/1/23/1752/008
Product Form: plv iol 10xdávka+10xsolv. (liek.inj.skl.+ liek.inj.skl.)
MA Status: E - Valid centralised marketing authorisation
Type of procedure: EU
MAH, country: Pfizer Europe MA EEIG, Belgium
Therapeutic Class: 59 - IMMUNOPRAEPARATA
ATC:
J ANTIINFECTIVES FOR SYSTEMIC USE
J07 VACCINES
J07B VIRAL VACCINES
J07BX Other viral vaccines
J07BX05 Respiratory syncytial virus vaccines
Shelf life: 36
Container: glass vial
Route of admin.: Intramuscular use
Prescription Status: Medicinal product subject to medical prescription.
Legal basis: Article 8(3) application - new active substance
MA issued: 23.08.2023
Validity: 23.08.2028
SmPC + PL: European Medicines Agency's database
Safety feature Yes
Data update: 17.09.2024
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