VANGUARD PLUS 7
VANGUARD PLUS 7
Authorised
- Canine parainfluenza virus, strain NL-CPI-5, Live
- Canine distemper virus, strain N-CDV, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine parvovirus, strain NL-35-D, Live
- Leptospira interrogans, serogroup Canicola, serovar Canicola, strain C51, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated
Product identification
Medicine name:
VANGUARD PLUS 7
Active substance:
- Canine parainfluenza virus, strain NL-CPI-5, Live
- Canine distemper virus, strain N-CDV, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine parvovirus, strain NL-35-D, Live
- Leptospira interrogans, serogroup Canicola, serovar Canicola, strain C51, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated
Target species:
-
Dog
-
Dog
Route of administration:
-
Subcutaneous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine parainfluenza virus, strain NL-CPI-5, Live6.00log10 cell culture infective dose 501.00millilitre(s)
-
Canine distemper virus, strain N-CDV, Live3.00log10 cell culture infective dose 501.00millilitre(s)
-
Canine adenovirus 2, strain Manhattan, Live3.20log10 cell culture infective dose 501.00millilitre(s)
-
Canine parvovirus, strain NL-35-D, Live7.00log10 cell culture infective dose 501.00millilitre(s)
-
Leptospira interrogans, serogroup Canicola, serovar Canicola, strain C51, Inactivated40.00Protective Dose1.00millilitre(s)
-
Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated40.00Protective Dose1.00millilitre(s)
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Dog
-
-
Subcutaneous use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AJ02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Romania
Available in:
-
Romania
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
- 140019
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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Romanian (PDF)
Published on: 19/11/2024
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