Vanguard DA2PI-CPV Lyophilisat et solvant pour suspension injectable pour chiens
Vanguard DA2PI-CPV Lyophilisat et solvant pour suspension injectable pour chiens
Authorised
- Canine distemper virus, strain N-CDV, Live
- Canine parvovirus, strain NL-35-D, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine parainfluenza virus, strain NL-CPI-5, Live
Product identification
Medicine name:
Vanguard DA2PI-CPV Lyophilisat et solvant pour suspension injectable pour chiens
Vanguard DA2PI-CPV Lyophilisat und Lösungsmittel zur Herstellung einer Injektionssuspension
Active substance:
- Canine distemper virus, strain N-CDV, Live
- Canine parvovirus, strain NL-35-D, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine parainfluenza virus, strain NL-CPI-5, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine distemper virus, strain N-CDV, Live3.00log10 cell culture infective dose 501.00millilitre(s)
-
Canine parvovirus, strain NL-35-D, Live7.00log10 cell culture infective dose 501.00millilitre(s)
-
Canine adenovirus 2, strain Manhattan, Live3.20log10 cell culture infective dose 501.00millilitre(s)
-
Canine parainfluenza virus, strain NL-CPI-5, Live6.00log10 cell culture infective dose 501.00millilitre(s)
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AD04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Luxembourg
Available in:
-
Luxembourg
Package description:
- Vanguard DA2PI-CPV 1 dose Vial Lyophilisate and solvent for suspension for injection
- Vanguard DA2PI-CPV 10 1 dose Vial Lyophilisate and solvent for suspension for injection
- Vanguard DA2PI-CPV 100 1 dose Vial Lyophilisate and solvent for suspension for injection
- Vanguard DA2PI-CPV 25 1 dose Vial Lyophilisate and solvent for suspension for injection
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:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Ministere De La Sante Division De La Pharmacie Et Des Medicaments
Authorisation number:
- V 087/93/11/0351
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
French (PDF)
Published on: 16/01/2024
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