VANGUARD 7 sospensione iniettabile per cani
VANGUARD 7 sospensione iniettabile per cani
Authorised
- Canine adenovirus 2, strain Manhattan, Live
- Canine parainfluenza virus, strain NL-CPI-5, Live
- Canine parvovirus, strain NL-35-D, Live
- Canine distemper virus, strain N-CDV, Live
- Leptospira interrogans, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated
- Leptospira interrogans, serovar Canicola, strain C51, Inactivated
Product identification
Medicine name:
VANGUARD 7 sospensione iniettabile per cani
Active substance:
- Canine adenovirus 2, strain Manhattan, Live
- Canine parainfluenza virus, strain NL-CPI-5, Live
- Canine parvovirus, strain NL-35-D, Live
- Canine distemper virus, strain N-CDV, Live
- Leptospira interrogans, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated
- Leptospira interrogans, serovar Canicola, strain C51, Inactivated
Target species:
-
Dog
Route of administration:
-
Intramuscular use
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine adenovirus 2, strain Manhattan, Live3.20/log10 50% cell culture infectious dose1.00millilitre(s)
-
Canine parainfluenza virus, strain NL-CPI-5, Live6.00/log10 50% cell culture infectious dose1.00millilitre(s)
-
Canine parvovirus, strain NL-35-D, Live7.00/log10 50% cell culture infectious dose1.00millilitre(s)
-
Canine distemper virus, strain N-CDV, Live3.00/log10 50% cell culture infectious dose1.00millilitre(s)
-
Leptospira interrogans, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated463.00/relative unit(s)1.00millilitre(s)
-
Leptospira interrogans, serovar Canicola, strain C51, Inactivated420.00/relative unit(s)1.00millilitre(s)
Pharmaceutical form:
-
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:
-
Italy
Available in:
-
Italy
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 Italia S.r.l
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
- Haupt Pharma Latina 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
Combined File of all Documents
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Italian (PDF)
Published on: 23/03/2023