Veterinary Medicines

BOVILIS BOVIPAST RSP, suspenzija za injekciju, goveda

Authorised
  • Mannheimia haemolytica, serotype A1, strain M4/1, Inactivated
  • Bovine parainfluenza virus 3, strain SF-4, Inactivated
  • Bovine respiratory syncytial virus, strain EV 908, Inactivated
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Product identification

Medicine name:
BOVILIS BOVIPAST RSP, suspenzija za injekciju, goveda
Active substance:
  • Mannheimia haemolytica, serotype A1, strain M4/1, Inactivated
  • Bovine parainfluenza virus 3, strain SF-4, Inactivated
  • Bovine respiratory syncytial virus, strain EV 908, Inactivated
Target species:
  • Cattle
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Mannheimia haemolytica, serotype A1, strain M4/1, Inactivated
    9000000000.00
    cells
    /
    5.00
    millilitre(s)
  • Bovine parainfluenza virus 3, strain SF-4, Inactivated
    7.30
    log10 50% tissue culture infectious dose
    /
    5.00
    millilitre(s)
  • Bovine respiratory syncytial virus, strain EV 908, Inactivated
    5.50
    log10 50% tissue culture infectious dose
    /
    5.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AL04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Croatia
Package description:

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 International B.V. Subsidiary In The Republic Of Croatia
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Ministry Of Agriculture Veterinary And Food Safety Directorate
Authorisation number:
  • UP/I-322-05/22-01/80
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Croatian (PDF)
Published on: 20/05/2025
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