Veterinary Medicines

Bovilis BVD Suspension for injection for cattle

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
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, 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
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Cattle (for meat production)
      • Meat and offal
        no withdrawal period
    • Cattle (dairy cow)
      • Milk
        no withdrawal period
      • Meat and offal
        no withdrawal period
    • Cattle (calf)
      • Meat and offal
        no withdrawal period
    • Cattle (heifer)
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
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:
  • Ministry Of Health
Authorisation number:
  • 102883
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)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 22/07/2024
Download