Veterinary Medicine Information website

Bovilis Bovivac S suspension for injection for cattle

Authorised
  • Salmonella enterica, subsp. enterica, serovar Dublin, strain S342/70, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain S341/70, Inactivated
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Product identification

Medicine name:
Bovilis Bovivac S suspension for injection for cattle
Active substance:
  • Salmonella enterica, subsp. enterica, serovar Dublin, strain S342/70, Inactivated
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain S341/70, Inactivated
Target species:
  • Cattle
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Salmonella enterica, subsp. enterica, serovar Dublin, strain S342/70, Inactivated
    10000000.00
    cells
    /
    0.01
    millilitre(s)
  • Salmonella enterica, subsp. enterica, serovar Typhimurium, strain S341/70, Inactivated
    10000000.00
    cells
    /
    0.01
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AB
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • Polyethylene multidose bottles (50 ml) with rubber stoppers sealed with an aluminium crimp cap. The containers and closurescomply with the Ph. Eur

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
  • MSD Animal Health UK Ltd
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/165/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0436/001
Concerned member states:
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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