Rispoval Lactovac C vakcina A.U.V.
Rispoval Lactovac C vakcina A.U.V.
Authorised
- Bovine rotavirus, strain 1005/78, Inactivated
- Bovine rotavirus, strain Holland, Inactivated
- Bovine coronavirus, strain 800, Inactivated
- Escherichia coli, serotype O9:K35 (fimbrial adhesin F5 and F41), strain S1091/83, Inactivated
Product identification
Medicine name:
Rispoval Lactovac C vakcina A.U.V.
Active substance:
- Bovine rotavirus, strain 1005/78, Inactivated
- Bovine rotavirus, strain Holland, Inactivated
- Bovine coronavirus, strain 800, Inactivated
- Escherichia coli, serotype O9:K35 (fimbrial adhesin F5 and F41), strain S1091/83, Inactivated
Target species:
-
Cattle
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Bovine rotavirus, strain 1005/78, Inactivated7.40log10 tissue culture infective dose 501.00unit(s)/dose
-
Bovine rotavirus, strain Holland, Inactivated7.00log10 tissue culture infective dose 501.00unit(s)/dose
-
Bovine coronavirus, strain 800, Inactivated5.80log10 tissue culture infective dose 501.00unit(s)/dose
-
Escherichia coli, serotype O9:K35 (fimbrial adhesin F5 and F41), strain S1091/83, Inactivated250.00haemagglutinating units1.00unit(s)/dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
- Cattle
-
Meat and offal0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AL02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
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:
- Zoetis Hungary Kft.
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Directorate Of Veterinary Medicinal Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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