Nobivac Ducat Lyophilisate and solvent for suspension for injection
Nobivac Ducat Lyophilisate and solvent for suspension for injection
Not 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
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, Live4.80/log10 50% tissue culture infectious dose1.00Dose
-
Feline calicivirus, strain F9, Live4.60/log10 plaque forming unit(s)1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI06AD03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Greece
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
Legal basis of product authorisation:
-
Immunological veterinary medicinal product application (Article 13d of Directive No 2001/82/EC)
Marketing authorisation holder:
- Intervet Hellas M.A.E.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 24691/15-04-2010/K-0169801
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0207/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet