Veterinary Medicine Information website

Avishield IB H120, lyophilisate for oculonasal suspension/use in drinking water, for chickens

Authorised
  • Infectious bronchitis virus, type Massachusetts, strain H120, Live
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Product identification

Medicine name:
Avishield IB H120, lyophilisate for oculonasal suspension/use in drinking water, for chickens
Active substance:
  • Infectious bronchitis virus, type Massachusetts, strain H120, Live
Target species:
  • Chicken
Route of administration:
  • Oculonasal use
  • In drinking water use

Product details

Active substance and strength:
  • Infectious bronchitis virus, type Massachusetts, strain H120, Live
    3.50
    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
      • Meat and offal
        0
        day
  • In drinking water use
    • Chicken
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI01AD07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
Available in:
  • Austria
Package description:
  • Carton box with 10 vials of 5000 doses of vaccine. Colourless glass vials (type I), which are closed with bromobutyl rubber stoppers and sealed with aluminium caps.
  • Carton box with 10 vials of 2500 doses of vaccine. Colourless glass vials (type I), which are closed with bromobutyl rubber stoppers and sealed with aluminium caps.
  • Carton box with 10 vials of 1000 doses of vaccine. Colourless glass vials (type I), which are closed with bromobutyl rubber stoppers and sealed with aluminium caps.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Izo S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Genera d.d.
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 838226
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0292/001
Concerned member states:
  • Austria
  • Belgium
  • Croatia
  • Czechia
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 2/03/2026
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 2/03/2026
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Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 2/03/2026
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Combined File of all Documents

English (PDF)
Published on: 6/03/2026
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