Covexin 8
Covexin 8
Authorised
- Clostridium novyi, type B, toxoid
- Clostridium chauvoei, Inactivated
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type B, beta toxoid
- Clostridium septicum, toxoid
- Tetanus toxoid adsorbed
- Clostridium haemolyticum, toxoid
Product identification
Medicine name:
Covexin 8
Active substance:
- Clostridium novyi, type B, toxoid
- Clostridium chauvoei, Inactivated
- Clostridium perfringens, type D, epsilon toxoid
- Clostridium perfringens, type C, beta toxoid
- Clostridium perfringens, type B, beta toxoid
- Clostridium septicum, toxoid
- Tetanus toxoid adsorbed
- Clostridium haemolyticum, toxoid
Target species:
-
Cattle
-
Pig
-
Sheep
Route of administration:
-
Subcutaneous use
Product details
Active substance and strength:
-
Clostridium novyi, type B, toxoid3.50international unit(s)1.00millilitre(s)
-
Clostridium chauvoei, Inactivated5.00international unit(s)1.00millilitre(s)
-
Clostridium perfringens, type D, epsilon toxoid5.00international unit(s)1.00millilitre(s)
-
Clostridium perfringens, type C, beta toxoid10.00international unit(s)1.00millilitre(s)
-
Clostridium perfringens, type B, beta toxoid10.00international unit(s)1.00millilitre(s)
-
Clostridium septicum, toxoid2.50international unit(s)1.00millilitre(s)
-
Tetanus toxoid adsorbed2.50international unit(s)1.00millilitre(s)
-
Clostridium haemolyticum, toxoid10.00international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Suspension for injection
Withdrawal period by route of administration:
-
Subcutaneous use
-
Cattle
-
Meat and offal0day
-
Milk0day
-
-
Pig
-
Meat and offal0day
-
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QI02AB01
- QI04AB01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
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:
- Zoetis Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Paul-Ehrlich-Institut
Authorisation number:
- A263/79
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
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 9/03/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 26/02/2024
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