Eurican DAPPi-L
Eurican DAPPi-L
Not authorised
- Canine distemper virus, strain BA5, Live
- Canine adenovirus 2, strain DK13, Live
- Canine parvovirus, strain CAG2, Live
- Canine parainfluenza virus, strain CGF 2004/75, Live
- Leptospira interrogans, serovar Canicola, strain 16070, Inactivated
- Leptospira interrogans, serovar Icterohaemorrhagiae, strain 16069, Inactivated
Product identification
Medicine name:
Eurican DAPPi-L
Active substance:
- Canine distemper virus, strain BA5, Live
- Canine adenovirus 2, strain DK13, Live
- Canine parvovirus, strain CAG2, Live
- Canine parainfluenza virus, strain CGF 2004/75, Live
- Leptospira interrogans, serovar Canicola, strain 16070, Inactivated
- Leptospira interrogans, serovar Icterohaemorrhagiae, strain 16069, Inactivated
Target species:
-
Dog
-
Dog
Route of administration:
-
Subcutaneous use
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine distemper virus, strain BA5, Live1000000.00/50% tissue culture infectious dose1.00Dose
-
Canine adenovirus 2, strain DK13, Live1995260.00/50% tissue culture infectious dose1.00Dose
-
Canine parvovirus, strain CAG2, Live12589300.00/50% tissue culture infectious dose1.00Dose
-
Canine parainfluenza virus, strain CGF 2004/75, Live12589300.00/50% tissue culture infectious dose1.00Dose
-
Leptospira interrogans, serovar Canicola, strain 16070, Inactivated80.00/Hamster protective Dose 80%1.00millilitre(s)
-
Leptospira interrogans, serovar Icterohaemorrhagiae, strain 16069, Inactivated80.00/Hamster protective Dose 80%1.00millilitre(s)
Pharmaceutical form:
-
Lyophilisate and suspension 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:
-
Germany
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 Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Paul-Ehrlich-Institut
Authorisation number:
- 194a/97
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
German (PDF)
Published on: 14/04/2022