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VANGUARD 7 liofilizado y suspension para suspension inyectable para perros

Authorised
  • Canine distemper virus, strain N-CDV, Live
  • Canine adenovirus 2, strain Manhattan, Live
  • Canine parainfluenza virus, strain NL-CPI-5, Live
  • Canine parvovirus, strain NL-35-D, Live
  • Leptospira interrogans, serovar Canicola, strain C51, Inactivated
  • Leptospira interrogans, serovar Canicola, strain C51, Inactivated
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Product identification

Medicine name:
VANGUARD 7 liofilizado y suspension para suspension inyectable para perros
Active substance:
  • Canine distemper virus, strain N-CDV, Live
  • Canine adenovirus 2, strain Manhattan, Live
  • Canine parainfluenza virus, strain NL-CPI-5, Live
  • Canine parvovirus, strain NL-35-D, Live
  • Leptospira interrogans, serovar Canicola, strain C51, Inactivated
  • Leptospira interrogans, serovar Canicola, strain C51, Inactivated
Target species:
  • Dog
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Canine distemper virus, strain N-CDV, Live
    3.00
    50% cell culture infectious dose
    /
    1.00
    Dose
  • Canine adenovirus 2, strain Manhattan, Live
    3.20
    50% cell culture infectious dose
    /
    1.00
    Dose
  • Canine parainfluenza virus, strain NL-CPI-5, Live
    6.00
    50% cell culture infectious dose
    /
    1.00
    Dose
  • Canine parvovirus, strain NL-35-D, Live
    7.00
    50% cell culture infectious dose
    /
    1.00
    Dose
  • Leptospira interrogans, serovar Canicola, strain C51, Inactivated
    80.00
    percentage protection
    /
    1.00
    Dose
  • Leptospira interrogans, serovar Canicola, strain C51, Inactivated
    80.00
    percentage protection
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and suspension 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:
  • Spain
Available in:
  • Spain
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Zoetis Spain S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 3121 ESP
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Spanish (PDF)
Published on: 29/11/2023
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 29/11/2023
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 29/11/2023
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