Vanguard CPV-Lepto
Vanguard CPV-Lepto
Authorised
- Canine parvovirus, strain NL-35-D, Live
- Leptospira interrogans, serogroup Canicola, serovar Canicola, strain C51, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated
Product identification
Medicine name:
Vanguard CPV-Lepto
Active substance:
- Canine parvovirus, strain NL-35-D, Live
- Leptospira interrogans, serogroup Canicola, serovar Canicola, strain C51, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine parvovirus, strain NL-35-D, Live8.50log10 cell culture infective dose 501.00Vial
-
Leptospira interrogans, serogroup Canicola, serovar Canicola, strain C51, Inactivated422.00unit(s)1.00Dose
-
Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, strain NADL 11403, Inactivated493.00unit(s)1.00Dose
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI05
Legal status of supply:
-
Medicinal product subject to medical prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Package description:
- Blister met 25 glazen (Type I) injectieflacons met rubberstop en metalen felscapsule à 1 dosis vaccin.
- Blister met 100 glazen (Type I) injectieflacons met rubberstop en metalen felscapsule à 1 dosis vaccin.
- Blister met 10 glazen (Type I) injectieflacons met rubberstop en metalen felscapsule à 1 dosis vaccin.
- Blister met 1 glazen (Type I) injectieflacon met rubberstop en metalen felscapsule à 1 dosis vaccin.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Zoetis B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- MEB
Authorisation number:
- REG NL 8371
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Dutch (PDF)
Published on: 29/03/2023
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