Nobivac L+DHPPi lyofilisaat en suspensie voor suspensie voor injectie voor honden
Nobivac L+DHPPi lyofilisaat en suspensie voor suspensie voor injectie voor honden
Authorised
- Canine distemper virus, strain Onderstepoort, Live
- Canine parainfluenza virus, strain Cornell, Live
- Canine parvovirus, strain 154, Live
- Canine adenovirus 2, strain Manhattan LPV3, Live
- Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, Inactivated
- Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, Inactivated
Product identification
Medicine name:
Nobivac L+DHPPi lyofilisaat en suspensie voor suspensie voor injectie voor honden
Active substance:
- Canine distemper virus, strain Onderstepoort, Live
- Canine parainfluenza virus, strain Cornell, Live
- Canine parvovirus, strain 154, Live
- Canine adenovirus 2, strain Manhattan LPV3, Live
- Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, Inactivated
- Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, Inactivated
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine distemper virus, strain Onderstepoort, Live4.00/log10 50% cell culture infectious dose1.00millilitre(s)
-
Canine parainfluenza virus, strain Cornell, Live5.50/log10 50% cell culture infectious dose1.00millilitre(s)
-
Canine parvovirus, strain 154, Live7.00/log10 50% cell culture infectious dose1.00millilitre(s)
-
Canine adenovirus 2, strain Manhattan LPV3, Live4.00/log10 50% cell culture infectious dose1.00millilitre(s)
-
Leptospira interrogans, serovar Portlandvere, strain Ca-12-000, Inactivated1300.00/enzyme-linked immunosorbent assay unit/millilitre1.00millilitre(s)
-
Leptospira interrogans, serovar Copenhageni, strain Ic-02-001, Inactivated750.00/enzyme-linked immunosorbent assay unit/millilitre1.00millilitre(s)
Pharmaceutical form:
-
Lyophilisate for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Netherlands
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Intervet Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet Nederland B.V.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 9483
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 6/02/2025