PA-OLVAC +I+E Vaccino inattivato in emulsione iniettabile per tacchini
PA-OLVAC +I+E Vaccino inattivato in emulsione iniettabile per tacchini
Authorised
- Haemorrhagic enteritis virus, Inactivated
- Newcastle disease virus, Inactivated
- Riemerella anatipestifer, serotype 1, Inactivated
- Riemerella anatipestifer, serotype 3, Inactivated
- Avian influenza A virus H9N2, Inactivated
- Avian influenza A virus H6N2, Inactivated
Product identification
Medicine name:
PA-OLVAC +I+E Vaccino inattivato in emulsione iniettabile per tacchini
Active substance:
- Haemorrhagic enteritis virus, Inactivated
- Newcastle disease virus, Inactivated
- Riemerella anatipestifer, serotype 1, Inactivated
- Riemerella anatipestifer, serotype 3, Inactivated
- Avian influenza A virus H9N2, Inactivated
- Avian influenza A virus H6N2, Inactivated
Target species:
-
Turkey
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Haemorrhagic enteritis virus, Inactivated1733.00enzyme-linked immunosorbent assay unit0.50millilitre(s)
-
Newcastle disease virus, Inactivated50.0050% Protective Dose0.50millilitre(s)
-
Riemerella anatipestifer, serotype 1, Inactivated1.00billion colony forming units0.50millilitre(s)
-
Riemerella anatipestifer, serotype 3, Inactivated1.00billion colony forming units0.50millilitre(s)
-
Avian influenza A virus H9N2, Inactivated
-
Avian influenza A virus H6N2, Inactivated
Pharmaceutical form:
-
Emulsion for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Turkey
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI01CL01
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
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
Combined File of all Documents
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Italian (PDF)
Published on: 3/06/2022
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