EURICAN DAPPI-L, κόνις και διαλύτης για ενέσιμο εναιώρημα για σκύλους
EURICAN DAPPI-L, κόνις και διαλύτης για ενέσιμο εναιώρημα για σκύλους
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
- Canine parainfluenza virus 2, Inactivated
Product identification
Medicine name:
EURICAN DAPPI-L, κόνις και διαλύτης για ενέσιμο εναιώρημα για σκύλους
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
- Canine parainfluenza virus 2, Inactivated
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine distemper virus, strain BA5, Live10000.00cell culture infective dose 501.00millilitre(s)
-
Canine adenovirus 2, strain DK13, Live316.22cell culture infective dose 501.00millilitre(s)
-
Canine parvovirus, strain CAG2, Live79.43cell culture infective dose 501.00millilitre(s)
-
Canine parainfluenza virus, strain CGF 2004/75, Live50.12cell culture infective dose 501.00millilitre(s)
-
Canine parainfluenza virus 2, Inactivated
Pharmaceutical form:
-
Powder and solvent for suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AI02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 38630/27-04-2017/K-0225001
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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