Veterinary Medicines

Nobivac DHP lyofilisaat en suspendeervloeistof voor suspensie voor injectie voor honden

Authorised
  • Canine parvovirus, strain 154, Live
  • Canine adenovirus 2, strain Manhattan LPV3, Live
  • Canine distemper virus, strain Onderstepoort, Live
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Product identification

Medicine name:
Nobivac DHP lyofilisaat en suspendeervloeistof voor suspensie voor injectie voor honden
Active substance:
  • Canine parvovirus, strain 154, Live
  • Canine adenovirus 2, strain Manhattan LPV3, Live
  • Canine distemper virus, strain Onderstepoort, Live
Target species:
  • Dog
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Canine parvovirus, strain 154, Live
    7.00
    log10 50% cell culture infectious dose
    /
    1.00
    millilitre(s)
  • Canine adenovirus 2, strain Manhattan LPV3, Live
    4.00
    log10 50% cell culture infectious dose
    /
    1.00
    millilitre(s)
  • Canine distemper virus, strain Onderstepoort, Live
    4.00
    log10 50% cell culture infectious dose
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI07AD02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • Available only in Dutch
  • Available only in Dutch
  • Available only in Dutch
  • Available only in Dutch
  • Available only in Dutch
  • Available only in Dutch
  • Available only in Dutch
  • Kartonnen doos met 5 enkelvoudige doses.
  • Kartonnen doos met 5 enkelvoudige doses.
  • Kartonnen doos met 5 enkelvoudige doses.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Intervet Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 9477
Date of authorisation status change:

Documents

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Dutch (PDF)
Published on: 2/03/2022
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