Nobivac Pi, Lyophilisate and Solvent for Suspension for Injection for Dogs
Nobivac Pi, Lyophilisate and Solvent for Suspension for Injection for Dogs
Authorised
- Canine parainfluenza virus, strain Cornell, Live
Product identification
Medicine name:
Nobivac Pi, Lyophilisate and Solvent for Suspension for Injection for Dogs
Nobivac Pi vet. Frystorkat pulver och vätska till injektionsvätska, suspension
Active substance:
- Canine parainfluenza virus, strain Cornell, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine parainfluenza virus, strain Cornell, Live316228.0050% tissue culture infectious dose1.00Dose
Pharmaceutical form:
-
Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AD08
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Sweden
Package description:
- (ID4) 50 Dose; 50 millilitre(s): Box (Cardboard) with 50 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and 50 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID3) 25 Dose; 25 millilitre(s): Box (Cardboard) with 25 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and 25 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID2) 10 Dose; 10 millilitre(s): Box (Cardboard) with 10 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and 10 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID1) 5 Dose; 5 millilitre(s): Box (Cardboard) with 5 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and 5 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID16) 50 Dose; 50 millilitre(s): Box (Plastic) with 50 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and Box (Plastic) with 50 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID15) 25 Dose; 25 millilitre(s): Box (Plastic) with 25 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and Box (Plastic) with 25 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID14) 10 Dose; 10 millilitre(s): Box (Plastic) with 10 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and Box (Plastic) with 10 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID13) 5 Dose; 5 millilitre(s): Box (Plastic) with 5 Vial (Glass type I) each with 1 Dose, closed with Lid and Stopper (Aluminium, Halobutyl Rubber) and Box (Plastic) with 5 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID12) 50 Dose; 50 millilitre(s): Box (Cardboard) with 50 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and Box (Cardboard) with 50 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID11) 25 Dose; 25 millilitre(s): Box (Cardboard) with 25 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and Box (Cardboard) with 25 Vial (Glass type I) each with 1 Dose, closed with Lid and Stopper (Aluminium, Halobutyl Rubber)
- (ID10) 10 Dose; 10 millilitre(s): Box (Cardboard) with 10 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and Box (Cardboard) with 10 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID9) 5 Dose; 5 millilitre(s): Box (Cardboard) with 5 Vial (Glass type I) each with 1 Dose, closed with Lid and Stopper (Aluminium, Halobutyl Rubber) and Box (Cardboard) with 5 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID8) 50 Dose; 50 millilitre(s): Box (Plastic) with 50 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and 50 Vial (Glass type I) each with 1 millilitre(s), closed with Lid and Stopper (Aluminium, Halobutyl Rubber)
- (ID7) 25 Dose; 25 millilitre(s): Box (Plastic) with 25 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and 25 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID6) 10 Dose; 10 millilitre(s): Box (Plastic) with 10 Vial (Glass type I) each with 1 millilitre(s), closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and 10 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium)
- (ID5) 5 Dose; 5 millilitre(s): Box (Plastic) with 5 Vial (Glass type I) each with 1 Dose, closed with Stopper and Lid (Halobutyl Rubber, Aluminium) and 5 Vial (Glass type I) each with 1 millilitre(s), closed with Lid and Stopper (Aluminium, Halobutyl Rubber)
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:
- Swedish Medical Products Agency
Authorisation number:
- 18847
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0286/001
Concerned member states:
-
Austria
-
Belgium
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Greece
-
Hungary
-
Ireland
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Portugal
-
Slovenia
-
Sweden
-
United Kingdom (Northern Ireland)
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: 28/01/2022
Swedish (PDF)
Published on: 29/04/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Swedish (PDF)
Published on: 29/04/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Swedish (PDF)
Published on: 29/04/2025
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