Miloxan vakcina A.U.V.
Miloxan vakcina A.U.V.
Authorised
- Clostridium sordellii, toxoid
- Clostridium tetani, toxoid
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- Clostridium chauvoei, Inactivated
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type B and C, beta toxoid
Product identification
Medicine name:
Miloxan vakcina A.U.V.
Active substance:
- Clostridium sordellii, toxoid
- Clostridium tetani, toxoid
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- Clostridium chauvoei, Inactivated
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type B and C, beta toxoid
Target species:
-
Cattle
-
Sheep
-
Goat
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clostridium sordellii, toxoid1.00/90% protective dose in guinea pig1.00unit(s)/dose
-
Clostridium tetani, toxoid2.50/international unit(s)1.00unit(s)/dose
-
Clostridium septicum, toxoid2.50/international unit(s)1.00unit(s)/dose
-
Clostridium novyi, toxoid3.50/international unit(s)1.00unit(s)/dose
-
Clostridium chauvoei, Inactivated1.00/90% protective dose in guinea pig1.00unit(s)/dose
-
Clostridium perfringens, type D, epsilon toxoid5.00/international unit(s)1.00unit(s)/dose
-
Clostridium perfringens, type B and C, beta toxoid10.00/international unit(s)1.00unit(s)/dose
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Goat
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AB01
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:
- Boehringer Ingelheim Animal Health France
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
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