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Veterinary Medicines

Nobivac Ducat Lyophilisate and solvent for suspension for injection

Authorised
  • Felid herpesvirus 1, strain G2620A, Live
  • Feline calicivirus, strain F9, Live

Product identification

Medicine name:
Nobivac Ducat Lyophilisate and solvent for suspension for injection
Nobivac Ducat vet. Frystorkat pulver och vätska till injektionsvätska, suspension
Active substance:
  • Felid herpesvirus 1, strain G2620A, Live
  • Feline calicivirus, strain F9, Live
Target species:
  • Cat
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Felid herpesvirus 1, strain G2620A, Live
    4.80
    log10 50% tissue culture infectious dose
    /
    1.00
    Dose
  • Feline calicivirus, strain F9, Live
    4.60
    log10 plaque forming unit(s)
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI06AD03
Authorisation status:
  • Valid
Authorised in:
  • Sweden
Package description:
  • (ID44): 1 Cardbox with 50 Bottle (Glass) with 1 Dose and 50 Bottle (Glass) with 1 millilitre(s)) (50 Dose, 50 millilitre(s))
  • (ID34): 1 Cardbox with 25 Bottle (Glass) with 1 Dose and 25 Bottle (Glass) with 1 millilitre(s)) (25 Dose, 25 millilitre(s))
  • (ID24): 1 Cardbox with 10 Bottle (Glass) with 1 Dose and 10 Bottle (Glass) with 1 millilitre(s)) (10 Dose, 10 millilitre(s))
  • (ID14): 1 Cardbox 5 Bottle (Glass) with 1 Dose and 5 Bottle (Glass) with 1 millilitre(s)) (5 Dose, 5 millilitre(s))
  • (ID45): 1 Plasticbox 5 Bottle (Glass) with 1 Dose and 5 Bottle (Glass) with 1 millilitre(s)) (5 Dose, 5 millilitre(s))
  • (ID46): 1 Plasticbox with 10 Bottle (Glass) with 1 Dose and 10 Bottle (Glass) with 1 millilitre(s)) (10 Dose, 10 millilitre(s))
  • (ID47): 1 Plasticbox with 25 Bottle (Glass) with 1 Dose and 25 Bottle (Glass) with 1 millilitre(s)) (10 Dose, 10 millilitre(s))
  • (ID48): 1 Plasticbox with 50 Bottle (Glass) with 1 Dose and 50 Bottle (Glass) with 1 millilitre(s)) (10 Dose, 10 millilitre(s))

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Swedish Medical Products Agency
Authorisation number:
  • 25202
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0207/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Greece
  • Ireland
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 13/03/2023
Download
Swedish (PDF)
Published on: 3/05/2023

Package Leaflet

English (PDF)
Published on: 16/03/2023
Download
Swedish (PDF)
Published on: 3/05/2023

Labelling

This document does not exist in this language (English). You can find it in another language below.
Swedish (PDF)
Published on: 3/05/2023