Veterinary Medicines

Nobivac Ducat Lyophilisate and solvent for suspension for injection

Not authorised
  • Feline calicivirus, strain F9, Live
  • Felid herpesvirus 1, strain G2620A, Live
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Product identification

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

Product details

Active substance and strength:
  • Feline calicivirus, strain F9, Live
    0.66
    plaque forming unit
    /
    1.00
    Dose
  • Felid herpesvirus 1, strain G2620A, Live
    0.68
    plaque forming unit
    /
    1.00
    Dose
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI06AD03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Estonia
Package description:
  • (ID44): 1 Box with 50 Box with (1 Bottle (Glass) with 1 Dose and 1 Bottle (Glass) with 1 millilitre(s)) (50 Dose, 50 millilitre(s))
  • (ID34): 1 Box with 25 Box with (1 Bottle (Glass) with 1 Dose and 1 Bottle (Glass) with 1 millilitre(s)) (25 Dose, 25 millilitre(s))
  • (ID24): 1 Box with 10 Box with (1 Bottle (Glass) with 1 Dose and 1 Bottle (Glass) with 1 millilitre(s)) (10 Dose, 10 millilitre(s))
  • (ID14): 1 Box with 5 Box with (1 Bottle (Glass) with 1 Dose and 1 Bottle (Glass) with 1 millilitre(s)) (5 Dose, 5 millilitre(s))

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • State Agency Of Medicines
Authorisation number:
  • 1531
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0207/001

Documents

Summary of Product Characteristics

English (PDF)
Published on: 13/03/2023
Download
Estonian (PDF)
Published on: 14/08/2023
Updated on: 15/08/2023
Download

Package Leaflet

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