Veterinary Medicines

Bovilis IBR Marker Inac Suspension for Injection for Cattle

Authorised
  • Bovine herpesvirus 1, strain GK/D gE gene-deleted, Inactivated
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Product identification

Medicine name:
Bovilis IBR marker inac suspension for injection for cattle
Bovilis IBR Marker Inac Suspension for Injection for Cattle
Active substance:
  • Bovine herpesvirus 1, strain GK/D gE gene-deleted, Inactivated
Target species:
  • Cattle
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Bovine herpesvirus 1, strain GK/D gE gene-deleted, Inactivated
    60.00
    enzyme-linked immunosorbent assay unit
    /
    2.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AA03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
Package description:
  • (ID27) 2000 millilitre(s): Box (Cardboard) with 10 Bottle (PolyEthylene TerePhthalate) each with 200 millilitre(s)
  • (ID26) 2000 millilitre(s): Box (Cardboard) with 10 Bottle (Glass) each with 200 millilitre(s)
  • (ID25) 200 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 200 millilitre(s)
  • (ID24) 200 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 200 millilitre(s)
  • (ID23) 1000 millilitre(s): Box (Cardboard) with 10 Bottle (PolyEthylene TerePhthalate) each with 100 millilitre(s)
  • (ID22) 1000 millilitre(s): Box (Cardboard) with 10 Bottle (Glass) each with 100 millilitre(s)
  • (ID21) 100 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 100 millilitre(s)
  • (ID20) 100 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 100 millilitre(s)
  • (ID19) 500 millilitre(s): Box (Cardboard) with 10 Bottle (PolyEthylene TerePhthalate) each with 50 millilitre(s)
  • (ID17) 500 millilitre(s): Box (Cardboard) with 10 Bottle (Glass) each with 50 millilitre(s)
  • (ID15) 50 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 50 millilitre(s)
  • (ID10) 50 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 50 millilitre(s)
  • (ID9) 200 millilitre(s): Box (Cardboard) with 10 Bottle (PolyEthylene TerePhthalate) each with 20 millilitre(s)
  • (ID8) 200 millilitre(s): Box (Cardboard) with 10 Bottle (Glass) each with 20 millilitre(s)
  • (ID7) 20 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 20 millilitre(s)
  • (ID6) 20 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 20 millilitre(s)
  • (ID4) 100 millilitre(s): Box (Cardboard) with 10 Bottle (PolyEthylene TerePhthalate) each with 10 millilitre(s)
  • (ID3) 100 millilitre(s): Box (Cardboard) with 10 Bottle (Glass) each with 10 millilitre(s)
  • (ID2) 10 millilitre(s): Box (Cardboard) with 1 Bottle (PolyEthylene TerePhthalate) with 10 millilitre(s)
  • (ID1) 10 millilitre(s): Box (Cardboard) with 1 Bottle (Glass) with 10 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:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 06376/3008
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0237/001
Concerned member states:
  • Belgium
  • Czechia
  • Estonia
  • France
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)