IZOVAC ND-EDS-IB – Emulsione iniettabile per polli
IZOVAC ND-EDS-IB – Emulsione iniettabile per polli
Authorised
- Newcastle disease virus, strain Ulster, Inactivated
- Eggdrop syndrome-1976 virus, strain V127, Inactivated
- Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Avian infectious bronchitis virus, strain D274, Inactivated
- Avian infectious bronchitis virus, strain D1466, Inactivated
Product identification
Medicine name:
IZOVAC ND-EDS-IB – Emulsione iniettabile per polli
Active substance:
- Newcastle disease virus, strain Ulster, Inactivated
- Eggdrop syndrome-1976 virus, strain V127, Inactivated
- Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated
- Avian infectious bronchitis virus, strain D274, Inactivated
- Avian infectious bronchitis virus, strain D1466, Inactivated
Target species:
-
Chicken (layer hen)
-
Chicken (for reproduction)
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Newcastle disease virus, strain Ulster, Inactivated50.00/50% Protective Dose0.50millilitre(s)
-
Eggdrop syndrome-1976 virus, strain V127, Inactivated1.00/European Pharmacopoeia Unit(s)0.50millilitre(s)
-
Avian infectious bronchitis virus, type Massachusetts, strain M41, Inactivated1.00/European Pharmacopoeia Unit(s)0.50millilitre(s)
-
Avian infectious bronchitis virus, strain D274, Inactivated1.00/European Pharmacopoeia Unit(s)0.50millilitre(s)
-
Avian infectious bronchitis virus, strain D1466, Inactivated1.00/European Pharmacopoeia Unit(s)0.50millilitre(s)
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Chicken (layer hen)
-
Meat and offal0day
-
Egg0day
-
-
Chicken (for reproduction)
-
Meat and offal0day
-
Egg0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01AA13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Izo S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
- Izo S.r.l.
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 20/10/2022