Vanguard Plus 7 vakcina A.U.V.
Vanguard Plus 7 vakcina A.U.V.
Authorised
- Leptospira interrogans, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated
- Leptospira interrogans, serovar Canicola, strain C51, Inactivated
- Canine parvovirus, strain NL-35-D, Live
- Canine parainfluenza virus, strain NL-CPI-5, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine distemper virus, Live
Product identification
Medicine name:
Vanguard Plus 7 vakcina A.U.V.
Active substance:
- Leptospira interrogans, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated
- Leptospira interrogans, serovar Canicola, strain C51, Inactivated
- Canine parvovirus, strain NL-35-D, Live
- Canine parainfluenza virus, strain NL-CPI-5, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine distemper virus, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Leptospira interrogans, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated40.00/log10 50% cell culture infectious dose1.00unit(s)/dose
-
Leptospira interrogans, serovar Canicola, strain C51, Inactivated40.00/log10 50% cell culture infectious dose1.00unit(s)/dose
-
Canine parvovirus, strain NL-35-D, Live7.00/log10 50% cell culture infectious dose1.00unit(s)/dose
-
Canine parainfluenza virus, strain NL-CPI-5, Live6.00/log10 50% cell culture infectious dose1.00unit(s)/dose
-
Canine adenovirus 2, strain Manhattan, Live3.20/log10 50% cell culture infectious dose1.00unit(s)/dose
-
Canine distemper virus, Live3.00/log10 50% cell culture infectious dose1.00unit(s)/dose
Pharmaceutical form:
-
Powder and solvent for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Available in:
-
Hungary
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Hungary Kft.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Directorate Of Veterinary Medicinal Products
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