Veterinary Medicines

Rispoval 4

Authorised
  • Bovine herpesvirus 1, strain Cooper, Inactivated
  • Bovine viral diarrhoea virus 1, strain 5960, Inactivated
  • Bovine viral diarrhoea virus 1, strain 6309, Inactivated
  • Bovine parainfluenza virus 3, strain RLB103, Live
  • Bovine respiratory syncytial virus, strain 375, Live
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Product identification

Medicine name:
Rispoval 4
Active substance:
  • Bovine herpesvirus 1, strain Cooper, Inactivated
  • Bovine viral diarrhoea virus 1, strain 5960, Inactivated
  • Bovine viral diarrhoea virus 1, strain 6309, Inactivated
  • Bovine parainfluenza virus 3, strain RLB103, Live
  • Bovine respiratory syncytial virus, strain 375, Live
Target species:
  • Cattle (calf)
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Bovine herpesvirus 1, strain Cooper, Inactivated
    2.00
    log2 serum neutralising unit(s)
    /
    5.00
    millilitre(s)
  • Bovine viral diarrhoea virus 1, strain 5960, Inactivated
    5.00
    log2 serum neutralising unit(s)
    /
    5.00
    millilitre(s)
  • Bovine viral diarrhoea virus 1, strain 6309, Inactivated
    5.00
    log2 serum neutralising unit(s)
    /
    5.00
    millilitre(s)
  • Bovine parainfluenza virus 3, strain RLB103, Live
    5.00
    log10 50% cell culture infectious dose
    /
    5.00
    millilitre(s)
  • Bovine respiratory syncytial virus, strain 375, Live
    5.00
    log10 50% cell culture infectious dose
    /
    5.00
    millilitre(s)
Pharmaceutical form:
  • Lyophilisate and solvent for suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle (calf)
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AH
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Portugal
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:
  • Zoetis Portugal Lda.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Belgium
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • N723/03DGV
Date of authorisation status change:

Documents

Combined File of all Documents

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Published on: 19/06/2023
Updated on: 26/06/2023
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