Veterinary Medicines

BOVALTO TRIVACTON 6

Not authorised
  • Escherichia coli, serotype O101 (fimbrial adhesin F41), Inactivated
  • Escherichia coli, serotype O78 (antigen 31A), Inactivated
  • Escherichia coli, serotype O101 (fimbrial adhesin F5), Inactivated
  • Bovine coronavirus, strain INRA, Inactivated
  • Escherichia coli, serotype O117 (antigen Y), Inactivated
  • Bovine rotavirus A, Inactivated
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Product identification

Medicine name:
BOVALTO TRIVACTON 6
Active substance:
  • Escherichia coli, serotype O101 (fimbrial adhesin F41), Inactivated
  • Escherichia coli, serotype O78 (antigen 31A), Inactivated
  • Escherichia coli, serotype O101 (fimbrial adhesin F5), Inactivated
  • Bovine coronavirus, strain INRA, Inactivated
  • Escherichia coli, serotype O117 (antigen Y), Inactivated
  • Bovine rotavirus A, Inactivated
Target species:
  • Cattle
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Escherichia coli, serotype O101 (fimbrial adhesin F41), Inactivated
    0.90
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Escherichia coli, serotype O78 (antigen 31A), Inactivated
    0.90
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Escherichia coli, serotype O101 (fimbrial adhesin F5), Inactivated
    0.90
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Bovine coronavirus, strain INRA, Inactivated
    1.50
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Escherichia coli, serotype O117 (antigen Y), Inactivated
    0.90
    log10 serum neutralising unit(s)
    /
    1.00
    millilitre(s)
  • Bovine rotavirus A, Inactivated
    2.00
    log10 haemagglutination inhibiting unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
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Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AL01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Italy
Package description:

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:
  • Boehringer Ingelheim Animal Health Italia S.p.A. In Breve Boehringer Ingelheim Ah It S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Boehringer Ingelheim Animal Health France
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

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Italian (PDF)
Published on: 7/03/2023
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