Avishield IBD plus, lyophilisate for use in drinking water, for chickens
Avishield IBD plus, lyophilisate for use in drinking water, for chickens
Authorised
- Infectious bursal disease virus, strain G6, Live
Product identification
Medicine name:
Avishield IBD plus, lyophilisate for use in drinking water, for chickens
Avishield IBD Plus, Lyofilizát pro podání v pitné vodě
Active substance:
- Infectious bursal disease virus, strain G6, Live
Target species:
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Infectious bursal disease virus, strain G6, Live1.90unit(s)1.00Dose
Pharmaceutical form:
-
Lyophilisate for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
- Chicken
-
All relevant tissues0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AD09
Legal status of supply:
This information is not available for this product.
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Package description:
- Cardboard box with 10 vials of 5,000 doses of vaccine. Colourless glass vials (type I) filled into 10 ml (5000 doses), which are closed with bromobutyl rubber stoppers and sealed with aluminium caps.
- Cardboard box with 10 vials of 2,500 doses of vaccine. Colourless glass vials (type I) filled into 10 ml (2500 doses), which are closed with bromobutyl rubber stoppers and sealed with aluminium caps.
- Cardboard box with 10 vials of 1,000 doses of vaccine. Colourless glass vials (type I) filled into 4 ml (1000 doses), 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:
- Genera d.d.
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera d.d.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicines
Authorisation number:
- 97/046/20-C
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0311/001
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
Czechia
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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: 8/04/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 8/04/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 8/04/2024
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