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 Suspension injectable
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, Inactivated50.00enzyme-linked immunosorbent assay unit2.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Intramuscular use
- Cattle
-
Milk0day
-
Meat and offal0day
-
- Cattle (for meat production)
-
Meat and offal0day
-
- Cattle (dairy cow)
-
Milk0day
-
Meat and offal0day
-
- Cattle (calf)
-
Meat and offal0day
-
- Cattle (heifer)
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Luxembourg
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:
- Ministere De La Sante Division De La Pharmacie Et Des Medicaments
Authorisation number:
- V/817/99/08/0644
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0211/001
Concerned member states:
-
Austria
-
Belgium
-
Denmark
-
France
-
Greece
-
Ireland
-
Italy
-
Luxembourg
-
Netherlands
-
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
Summary of Product Characteristics
English (PDF)
Download Published on: 28/01/2022
French (PDF)
Published on: 15/06/2022
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