Veterinary Medicines

Bovilis BVD Suspension for injection for cattle

Not authorised
  • Bovine viral diarrhoea virus 1, strain C-86, Inactivated
Download as PDF

Product identification

Medicine name:
Bovilis BVD Suspension for injection for cattle
Bovilis BVD injektionsvæske, suspension
Active substance:
  • Bovine viral diarrhoea virus 1, strain C-86, Inactivated
Target species:
  • Cattle
  • Cattle (for meat production)
  • Cattle (dairy cattle)
  • Cattle (calf)
  • Cattle (heifer)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Bovine viral diarrhoea virus 1, strain C-86, Inactivated
    50.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Cattle (for meat production)
      • Meat and offal
        0
        day
    • Cattle (dairy cattle)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Cattle (calf)
      • Meat and offal
        0
        day
    • Cattle (heifer)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Denmark
Package description:
  • (ID7): 1 Box with 1 Bottle (Glass) with 100 millilitre(s) (100 millilitre(s))
  • (ID6): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 50 millilitre(s) (50 millilitre(s))
  • (ID1): 1 Box with 1 Bottle (Glass) with 10 millilitre(s) (10 millilitre(s))
  • (ID20): 1 Box with 1 Bottle (Glass) with 2 millilitre(s) (2 millilitre(s))
  • (ID30): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 2 millilitre(s) (2 millilitre(s))
  • (ID3): 1 Box with 1 Bottle (Glass) with 20 millilitre(s) (20 millilitre(s))
  • (ID9): 1 Box with 1 Bottle (Glass) with 250 millilitre(s) (250 millilitre(s))
  • (ID4): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 20 millilitre(s) (20 millilitre(s))
  • (ID2): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 10 millilitre(s) (10 millilitre(s))
  • (ID5): 1 Box with 1 Bottle (Glass) with 50 millilitre(s) (50 millilitre(s))
  • (ID8): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 100 millilitre(s) (100 millilitre(s))
  • (ID10): 1 Box with 1 Bottle (PolyEthylene TerePhthalate) with 250 millilitre(s) (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:
  • Danish Medicines Agency
Authorisation number:
  • 39194
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0211/001

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
Download
Danish (PDF)
Published on: 9/07/2023
Download