Covexin 8 vet. injeksjonsvæske, suspensjon Vaksine mot klostridieinfeksjoner til sau og storfe (inaktivert, adsorbert)
Covexin 8 vet. injeksjonsvæske, suspensjon Vaksine mot klostridieinfeksjoner til sau og storfe (inaktivert, adsorbert)
Not authorised
- Clostridium tetani, toxoid
- Clostridium novyi, toxoid
- Clostridium septicum, toxoid
- Clostridium haemolyticum, toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type B and C, beta toxoid
- Clostridium chauvoei, Inactivated
Product identification
Medicine name:
Covexin 8 vet. injeksjonsvæske, suspensjon Vaksine mot klostridieinfeksjoner til sau og storfe (inaktivert, adsorbert)
Active substance:
- Clostridium tetani, toxoid
- Clostridium novyi, toxoid
- Clostridium septicum, toxoid
- Clostridium haemolyticum, toxoid
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type B and C, beta toxoid
- Clostridium chauvoei, Inactivated
Target species:
-
Sheep
-
Cattle
-
Sheep (lamb)
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clostridium tetani, toxoid1.60enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium novyi, toxoid2.10enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium septicum, toxoid2.80enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium haemolyticum, toxoid11.70enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium perfringens, type D, epsilon toxoid7.00enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium perfringens, type B and C, beta toxoid13.10enzyme-linked immunosorbent assay unit1.00millilitre(s)
-
Clostridium chauvoei, Inactivated90.00percentage protection1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Sheep
-
All relevant tissues0day
-
-
Cattle
-
All relevant tissues0day
-
-
Sheep (lamb)
-
All relevant tissues0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AB01
- QI04AB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Norway
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Zoetis Finland Oy
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Norwegian Medical Products Agency
Authorisation number:
- 95-3537
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.
Norwegian (PDF)
Published on: 16/03/2022
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