EURICAN DAPPi - LR liofilizat in suspenzija za pripravo suspenzije za injiciranje za pse
EURICAN DAPPi - LR liofilizat in suspenzija za pripravo suspenzije za injiciranje za pse
Authorised
- Rabies virus, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, Inactivated
- Leptospira interrogans, Serogroup Canicola, Live
- Canine parainfluenza virus, Live
- Canine parvovirus, Live
- Canine adenovirus 2, Live
- Canine distemper virus, Live
Product identification
Medicine name:
EURICAN DAPPi - LR liofilizat in suspenzija za pripravo suspenzije za injiciranje za pse
Active substance:
- Rabies virus, Inactivated
- Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, Inactivated
- Leptospira interrogans, Serogroup Canicola, Live
- Canine parainfluenza virus, Live
- Canine parvovirus, Live
- Canine adenovirus 2, Live
- Canine distemper virus, Live
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Rabies virus, Inactivated1.00international unit(s)1.00millilitre(s)
-
Leptospira interrogans, serogroup Icterohaemorrhagiae, serovar Icterohaemorrhagiae, Inactivated1.00European Pharmacopoeia Unit(s)1.00millilitre(s)
-
Leptospira interrogans, Serogroup Canicola, Live1.00European Pharmacopoeia Unit(s)1.00millilitre(s)
-
Canine parainfluenza virus, Live50118.00log10 tissue culture infective dose 501.00Dose
-
Canine parvovirus, Live79432.00log10 tissue culture infective dose 501.00Dose
-
Canine adenovirus 2, Live316.00log10 tissue culture infective dose 501.00Dose
-
Canine distemper virus, Live10000.00log10 tissue culture infective dose 501.00Dose
Pharmaceutical form:
-
Lyophilisate and suspension 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:
-
Slovenia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
- NP/V/0126/001
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
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 14/11/2021
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 14/11/2021
Labelling
This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 14/11/2021
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