FILAVAC VHD K C+V SUSPENSION FOR INJECTION FOR RABBITS
FILAVAC VHD K C+V SUSPENSION FOR INJECTION FOR RABBITS
Authorised
- Rabbit haemorrhagic disease virus, type 1, strain IM.507.SC.2011, Inactivated
- Rabbit haemorrhagic disease virus, type 2, strain LP.SV.2012, Inactivated
Product identification
Medicine name:
FILAVAC VHD K C+V SUSPENSION FOR INJECTION FOR RABBITS
Filavac VHD K C+V Suspensie voor injectie
Filavac VHD K C+V Suspension injectable
Filavac VHD K C+V Injektionssuspension
Active substance:
- Rabbit haemorrhagic disease virus, type 1, strain IM.507.SC.2011, Inactivated
- Rabbit haemorrhagic disease virus, type 2, strain LP.SV.2012, Inactivated
Target species:
-
Rabbit
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Rabbit haemorrhagic disease virus, type 1, strain IM.507.SC.2011, Inactivated1.0090% protective dose1.00Dose
-
Rabbit haemorrhagic disease virus, type 2, strain LP.SV.2012, Inactivated1.0090% protective dose1.00Dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Rabbit
-
All relevant tissuesno withdrawal periodWithdrawal period is 0 days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI08AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - New active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Filavie
Marketing authorisation date:
Manufacturing sites for batch release:
- Filavie
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V509217
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0315/001
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Finland
-
Germany
-
Greece
-
Hungary
-
Italy
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
Slovakia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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