Bovilis BVD Suspension for injection for cattle
Bovilis BVD Suspension for injection for cattle
Authorised
- Bovine viral diarrhoea virus 1, strain C-86, Inactivated
Product identification
Medicine name:
Bovilis BVD Suspension for injection for cattle
Bovilis BVD Suspensie voor injectie
Bovilis BVD Suspension injectable
Bovilis BVD Injektionssuspension
Active substance:
- Bovine viral diarrhoea virus 1, strain C-86, Inactivated
Target species:
-
Cattle
-
Cattle (for meat production)
-
Cattle (dairy cow)
-
Cattle (calf)
-
Cattle (heifer)
Route of administration:
-
Intramuscular use
Product details
Active substance and strength:
-
Bovine viral diarrhoea virus 1, strain C-86, Inactivated50.00/enzyme-linked immunosorbent assay unit2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
-
Cattle
-
Milkno withdrawal periodzero days
-
Meat and offalno withdrawal periodzero ays
-
-
Cattle (for meat production)
-
Meat and offalno withdrawal periodzero days
-
-
Cattle (dairy cow)
-
Milkno withdrawal periodzero days
-
Meat and offalno withdrawal periodzero days
-
-
Cattle (calf)
-
Meat and offalno withdrawal periodzero days
-
-
Cattle (heifer)
-
Meat and offalno withdrawal periodzero days
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- (ID7) 100 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 100 millilitre(s)
- (ID6) 50 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 50 millilitre(s)
- (ID1) 10 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 10 millilitre(s)
- (ID20) 2 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 2 millilitre(s)
- (ID30) 2 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 2 millilitre(s)
- (ID3) 20 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 20 millilitre(s)
- (ID9) 250 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 250 millilitre(s)
- (ID4) 20 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 20 millilitre(s)
- (ID2) 10 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 10 millilitre(s)
- (ID5) 50 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 50 millilitre(s)
- (ID8) 100 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 100 millilitre(s)
- (ID10) 250 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 250 millilitre(s)
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:
- Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Intervet International B.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0433/001
Concerned member states:
-
Austria
-
Belgium
-
France
-
Germany
-
Greece
-
Ireland
-
Italy
-
Luxembourg
-
Poland
-
Portugal
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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