Vanguard 7
Vanguard 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 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
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine parainfluenza virus, strain NL-CPI-5, Live8.00log10 cell culture infective dose 501.00Vial
-
Canine distemper virus, strain N-CDV, Live316228.00cell culture infective dose 501.00Vial
-
Canine adenovirus 2, strain Manhattan, Live158489.00cell culture infective dose 501.00Vial
-
Canine parvovirus, strain NL-35-D, Live8.50log10 cell culture infective dose 501.00Vial
-
Leptospira interrogans, serogroup Canicola, serovar Canicola, strain C51, Inactivated422.00unit(s)1.00Dose
-
Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated493.00unit(s)1.00Dose
Pharmaceutical form:
-
Lyophilisate for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Package description:
- Blister containing 25 glass (Type I) vials with rubber stopper and metal cap containing 1 dose of liquid vaccine fraction as suspending liquid and 1 dose of freeze-dried
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Zoetis B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 8369
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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Dutch (PDF)
Published on: 29/03/2023
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