EURICAN DAPPi-LR, liofilizatas ir suspensija injekcinei suspensijai ruošti šunims
EURICAN DAPPi-LR, liofilizatas ir suspensija injekcinei suspensijai ruošti šunims
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
Product identification
Medicine name:
EURICAN DAPPi-LR, liofilizatas ir suspensija injekcinei suspensijai ruošti šunims
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
Target species:
-
Dog
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Canine distemper virus, strain BA5, Live10000.00/50% cell culture infectious dose1.00Dose
-
Canine adenovirus 2, strain DK13, Live316.23/50% cell culture infectious dose1.00Dose
-
Canine parvovirus, strain CAG2, Live79432.80/50% cell culture infectious dose1.00Dose
-
Canine parainfluenza virus, strain CGF 2004/75, Live50118.70/50% cell culture infectious dose1.00Dose
Pharmaceutical form:
-
Lyophilisate and suspension for suspension for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI07AJ06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription except for some pack sizes
Authorisation status:
-
Surrendered
Authorised in:
-
Lithuania
Package description:
- Available only in Lithuanian
- Available only in Lithuanian
- Available only in Lithuanian
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:
- State Food And Veterinary Service
Authorisation number:
- LT/2/02/1378/001-003
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.
Lithuanian (PDF)
Published on: 7/12/2022