Versican Plus DP lyophilisate and solvent for suspension for injection for dogs
Versican Plus DP lyophilisate and solvent for suspension for injection for dogs
Authorised
- Canine parvovirus, type 2b, strain CPV-2b Bio 12/B, Live
- Canine distemper virus, strain CDV Bio 11/A, Live
Product identification
Medicine name:
Versican Plus DP lyophilisate and solvent for suspension for injection for dogs
Versican Plus DP λυοφιλοποιημένο υλικό και διαλύτης για ενέσιμο εναιώρημα για σκύλους
Active substance:
- Canine parvovirus, type 2b, strain CPV-2b Bio 12/B, Live
- Canine distemper virus, strain CDV Bio 11/A, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine parvovirus, type 2b, strain CPV-2b Bio 12/B, Live19952.00/50% tissue culture infectious dose1.00Dose
-
Canine distemper virus, strain CDV Bio 11/A, Live1258.00/50% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AD03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Package description:
- (ID2) 50 Dose; 50 millilitre(s): Box (plastics) with 50 Vial (glass) each with 1 Dose and 50 Vial (glass) each with 1 millilitre(s)
- (ID1) 25 Dose; 25 millilitre(s): Box (plastics) with 25 Vial (glass) each with 1 Dose and 25 Vial (glass) each with 1 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:
- Zoetis Hellas S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Bioveta a.s.
Responsible authority:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
- CY00539V
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0266/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Cyprus
-
Greece
-
Hungary
-
Italy
-
Lithuania
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet