Eurican DAPPi-LR vakcina
Eurican DAPPi-LR vakcina
Not authorised
- Leptospira interrogans, serovar Icterohaemorrhagiae, strain 16069, Inactivated
- Leptospira interrogans, serovar Canicola, strain 16070, Inactivated
- Rabies virus, Inactivated
- Canine parvovirus, Live
- Canine parainfluenza virus, Live
- Canine adenovirus 2, Live
- Canine distemper virus, Live
Product identification
Medicine name:
Eurican DAPPi-LR vakcina
Active substance:
- Leptospira interrogans, serovar Icterohaemorrhagiae, strain 16069, Inactivated
- Leptospira interrogans, serovar Canicola, strain 16070, Inactivated
- Rabies virus, Inactivated
- Canine parvovirus, Live
- Canine parainfluenza virus, Live
- Canine adenovirus 2, Live
- Canine distemper virus, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Leptospira interrogans, serovar Icterohaemorrhagiae, strain 16069, Inactivated40.00/Hamster protective Dose 80%1.00unit(s)/dose
-
Leptospira interrogans, serovar Canicola, strain 16070, Inactivated40.00/Hamster protective Dose 80%1.00unit(s)/dose
-
Rabies virus, Inactivated1.00/international unit(s)1.00unit(s)/dose
-
Canine parvovirus, Live4.90/log10 50% tissue culture infectious dose1.00unit(s)/dose
-
Canine parainfluenza virus, Live4.70/log10 50% tissue culture infectious dose1.00unit(s)/dose
-
Canine adenovirus 2, Live2.50/log10 50% tissue culture infectious dose1.00unit(s)/dose
-
Canine distemper virus, Live4.00/log10 50% tissue culture infectious dose1.00unit(s)/dose
Pharmaceutical form:
-
Powder and solvent for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Hungary
Package description:
- Available only in Hungarian
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:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France SCS
Responsible authority:
- Directorate Of Veterinary Medicinal Products
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