Vanguard plus 7 liofilizat in vehikel za raztopino za injiciranje za pse
Vanguard plus 7 liofilizat in vehikel za raztopino za injiciranje za pse
Authorised
- LEPTOSPIRA ICTEROHAEMORRHAGIAE INACTIVATED
- Leptospira interrogans, Serogroup Canicola, serovar Canicola, Inactivated
- Canine parvovirus, strain NL-35-D, Live
- Canine parainfluenza virus, strain NL-CPI-5, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine distemper virus, strain N-CDV, Live
Product identification
Medicine name:
Vanguard plus 7 liofilizat in vehikel za raztopino za injiciranje za pse
Active substance:
- LEPTOSPIRA ICTEROHAEMORRHAGIAE INACTIVATED
- Leptospira interrogans, Serogroup Canicola, serovar Canicola, Inactivated
- Canine parvovirus, strain NL-35-D, Live
- Canine parainfluenza virus, strain NL-CPI-5, Live
- Canine adenovirus 2, strain Manhattan, Live
- Canine distemper virus, strain N-CDV, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
LEPTOSPIRA ICTEROHAEMORRHAGIAE INACTIVATED40.00Protective Dose1.00millilitre(s)
-
Leptospira interrogans, Serogroup Canicola, serovar Canicola, Inactivated40.00Protective Dose1.00millilitre(s)
-
Canine parvovirus, strain NL-35-D, Live10000000.00cell culture infective dose 501.00millilitre(s)
-
Canine parainfluenza virus, strain NL-CPI-5, Live1000000.00cell culture infective dose 501.00Dose
-
Canine adenovirus 2, strain Manhattan, Live1584.00cell culture infective dose 501.00Dose
-
Canine distemper virus, strain N-CDV, Live1000.00cell culture infective dose 501.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovenia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0347/001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 10/11/2021
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 10/11/2021
Labelling
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 10/11/2021
How useful was this page?: