Veterinary Medicines

AviGate ND QV4 lyophilisate for oculonasal suspension/use in drinking water for chickens

Authorised
  • Newcastle disease virus, strain QV4, Live
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Product identification

Medicine name:
AviGate ND QV4 lyophilisate for oculonasal suspension/use in drinking water for chickens
Avigate ND QV4, Lyofilizát pro okulonazální suspenzi/pro podání v pitné vodě
Active substance:
  • Newcastle disease virus, strain QV4, Live
Target species:
  • Chicken
Route of administration:
  • Oculonasal use
  • In drinking water use

Product details

Active substance and strength:
  • Newcastle disease virus, strain QV4, Live
    6.00
    log 10 50% embryo infective dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate for oculonasal suspension/use in drinking water
Withdrawal period by route of administration:
  • Oculonasal use
    • Chicken
      • All relevant tissues
        0
        day
  • In drinking water use
    • Chicken
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Package description:
  • Carton box with 10 glass vials (type I) containing 1 000 doses, closed with a rubber stopper and sealed with an aluminium cap.
  • Carton box with 10 glass vials (type I) containing 2 500 doses, closed with a rubber stopper and sealed with an aluminium cap.
  • Carton box with 10 glass vials (type I) containing 5 000 doses, closed with a rubber stopper and sealed with an aluminium cap.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
  • HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
  • Biovet AD
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/012/26-C
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0435/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Czechia
  • Greece
  • Italy
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 9/02/2026
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 9/02/2026
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 9/02/2026
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