Covexin 10 Suspension for injection for sheep and cattle
Covexin 10 Suspension for injection for sheep and cattle
Authorised
- Clostridium haemolyticum, toxoid
- Clostridium sordellii, toxoid
- Tetanus toxoid adsorbed
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type B and C, beta toxoid
- Clostridium chauvoei, Inactivated
- Clostridium perfringens, type A and C, alpha toxoid
Product identification
Medicine name:
Covexin 10 Suspension for injection for sheep and cattle
COVEXIN 10, injekcinė suspensija avims ir galvijams
Active substance:
- Clostridium haemolyticum, toxoid
- Clostridium sordellii, toxoid
- Tetanus toxoid adsorbed
- Clostridium septicum, toxoid
- Clostridium novyi, toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type B and C, beta toxoid
- Clostridium chauvoei, Inactivated
- Clostridium perfringens, type A and C, alpha toxoid
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clostridium haemolyticum, toxoid16.50enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium sordellii, toxoid0.80enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Tetanus toxoid adsorbed2.50enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium septicum, toxoid3.60enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium novyi, toxoid1.20enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium perfringens, type D, epsilon toxoid5.10enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium perfringens, type B and C, beta toxoid12.40enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium chauvoei, Inactivated90.00percentage protection1.00millilitre(s)
-
Clostridium perfringens, type A and C, alpha toxoid0.90enzyme-linked immunosorbent assay unit1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
Milk0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AB01
- QI04AB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- (ID1) 2 millilitre(s): Box (Cardboard) with 1 Bottle (High Density PolyEthylene) with 2 millilitre(s)
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 Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
- Schering-Plough Limited
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/10/1859/002–003
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0283/001
Concerned member states:
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
France
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
How useful was this page?: