Nobivac CEPPi, liofilizzato per sospensione iniettabile per cani
Nobivac CEPPi, liofilizzato per sospensione iniettabile per cani
Authorised
- Canine parvovirus, strain 154, Live
- Canine parainfluenza virus, strain Cornell, Live
- Canine distemper virus, strain Onderstepoort, Live
- Canine adenovirus 2, strain Manhattan LPV3, Live
Product identification
Medicine name:
Nobivac CEPPi, liofilizzato per sospensione iniettabile per cani
Active substance:
- Canine parvovirus, strain 154, Live
- Canine parainfluenza virus, strain Cornell, Live
- Canine distemper virus, strain Onderstepoort, Live
- Canine adenovirus 2, strain Manhattan LPV3, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine parvovirus, strain 154, Live7.00log10 tissue culture infective dose 501.00unit(s)
-
Canine parainfluenza virus, strain Cornell, Live5.50log10 tissue culture infective dose 501.00unit(s)
-
Canine distemper virus, strain Onderstepoort, Live4.00log10 tissue culture infective dose 501.00unit(s)
-
Canine adenovirus 2, strain Manhattan LPV3, Live4.00log10 tissue culture infective dose 501.00unit(s)
Pharmaceutical form:
-
Lyophilisate for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Dog
-
Unspecified0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AD04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Ministry Of Health
Authorisation number:
This information is not available for this product.
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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in another language below.
Italian (PDF)
Published on: 3/06/2022
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