Veterinary Medicines

CANIGEN DHA2PPiL, Lyofilizát a rozpouštědlo pro injekční suspenzi

Authorised
  • Canine adenovirus 2, Live
  • Canine parainfluenza virus, Live
  • Canine parvovirus, Live
  • Canine distemper virus, Live
  • Leptospira interrogans, serogroup Canicola, serovar Canicola, strain 601903, Inactivated
  • Leptospira interrogans, serovar Icterohaemorrhagiae, strain 601895, Inactivated
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Product identification

Medicine name:
CANIGEN DHA2PPiL, Lyofilizát a rozpouštědlo pro injekční suspenzi
Active substance:
  • Canine adenovirus 2, Live
  • Canine parainfluenza virus, Live
  • Canine parvovirus, Live
  • Canine distemper virus, Live
  • Leptospira interrogans, serogroup Canicola, serovar Canicola, strain 601903, Inactivated
  • Leptospira interrogans, serovar Icterohaemorrhagiae, strain 601895, Inactivated
Target species:
  • Dog
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Canine adenovirus 2, Live
    6.00
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Canine parainfluenza virus, Live
    7.00
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Canine parvovirus, Live
    7.00
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Canine distemper virus, Live
    5.00
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Leptospira interrogans, serogroup Canicola, serovar Canicola, strain 601903, Inactivated
    40.00
    Protective Dose
    /
    1.00
    Dose
  • Leptospira interrogans, serovar Icterohaemorrhagiae, strain 601895, Inactivated
    40.00
    Protective Dose
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent 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:
  • Czechia
Package description:

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:
  • Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
  • Virbac
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 97/106/98-C
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Czech (PDF)
Published on: 26/10/2022
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Package Leaflet

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Czech (PDF)
Published on: 26/10/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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