Vanguard CPV solution for injection for dogs
Vanguard CPV solution for injection for dogs
Authorised
- Canine parvovirus, strain NL-35-D, Live
Product identification
Medicine name:
Vanguard CPV solution for injection for dogs
Active substance:
- Canine parvovirus, strain NL-35-D, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine parvovirus, strain NL-35-D, Live316228000.00/50% cell culture infectious dose1.00Dose
Pharmaceutical form:
-
Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AD01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Available in:
-
Ireland
Package description:
- The vaccine is filled in 1 dose vials glass type I (Ph.Eur.). Pack contains 100vials of 1 ml liquid Vanguard CPV.
- The vaccine is filled in 1 dose vials glass type I (Ph.Eur.). Pack contains 25vials of 1 ml liquid Vanguard CPV.
- The vaccine is filled in 1 dose vials glass type I (Ph.Eur.). Pack contains 10vials of 1 ml liquid Vanguard CPV.
- The vaccine is filled in 1 dose vials glass type I (Ph.Eur.). Pack contains 1vial of 1 ml liquid Vanguard CPV.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Zoetis Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10387/083/001
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
English (PDF)
Download Published on: 9/03/2025