Trivacton
Trivacton
Not authorised
- Bovine coronavirus, strain CR1, Inactivated
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Escherichia coli, serotypes O117 and O8 (antigen Y), Inactivated
- Escherichia coli, serotype O78 (antigen 31A), Inactivated
- Escherichia coli, serotype O101 (fimbrial adhesin F41), Inactivated
- Bovine rotavirus A, strain RoI, Inactivated
Product identification
Medicine name:
Trivacton
Active substance:
- Bovine coronavirus, strain CR1, Inactivated
- Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated
- Escherichia coli, serotypes O117 and O8 (antigen Y), Inactivated
- Escherichia coli, serotype O78 (antigen 31A), Inactivated
- Escherichia coli, serotype O101 (fimbrial adhesin F41), Inactivated
- Bovine rotavirus A, strain RoI, Inactivated
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Bovine coronavirus, strain CR1, Inactivated1.50/log10 serum neutralising unit(s)5.00millilitre(s)
-
Escherichia coli, serotype O101:K99 (fimbrial adhesin F5), Inactivated1.30/log10 slow agglutination unit(s)5.00millilitre(s)
-
Escherichia coli, serotypes O117 and O8 (antigen Y), Inactivated0.90/log10 slow agglutination unit(s)5.00millilitre(s)
-
Escherichia coli, serotype O78 (antigen 31A), Inactivated1.50/log10 slow agglutination unit(s)5.00millilitre(s)
-
Escherichia coli, serotype O101 (fimbrial adhesin F41), Inactivated0.60/log10 slow agglutination unit(s)5.00millilitre(s)
-
Bovine rotavirus A, strain RoI, Inactivated2.00/log10 haemagglutination inhibiting unit(s)5.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AL01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Germany
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 Vetmedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France SCS
Responsible authority:
- Paul-Ehrlich-Institut
Authorisation number:
- 520a/91
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
German (PDF)
Published on: 29/03/2022