Skip to main content
Veterinary Medicines

Bravoxin 10 suspension for injection for cattle and sheep

Not authorised
  • Clostridium perfringens, type A, alpha toxoid
  • Clostridium perfringens, type B, beta toxoid
  • Clostridium perfringens, type C, beta toxoid
  • Clostridium perfringens, type D, epsilon toxoid
  • Clostridium chauvoei, Inactivated
  • Clostridium novyi, toxoid
  • Clostridium septicum, toxoid
  • Tetanus toxoid adsorbed
  • Clostridium sordellii, toxoid
  • Clostridium novyi, type D, toxoid

Product identification

Medicine name:
Bravoxin 10 suspension for injection for cattle and sheep
Bravoxin 10 Suspensie voor injectie
Bravoxin 10 Suspension injectable
Bravoxin 10 Injektionssuspension
Active substance:
  • Clostridium perfringens, type A, alpha toxoid
  • Clostridium perfringens, type B, beta toxoid
  • Clostridium perfringens, type C, beta toxoid
  • Clostridium perfringens, type D, epsilon toxoid
  • Clostridium chauvoei, Inactivated
  • Clostridium novyi, toxoid
  • Clostridium septicum, toxoid
  • Tetanus toxoid adsorbed
  • Clostridium sordellii, toxoid
  • Clostridium novyi, type D, toxoid
Target species:
  • Cattle
  • Sheep
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Clostridium perfringens, type A, alpha toxoid
    0.50
    enzyme-linked immunosorbent assay unit
    /
    1.00
    millilitre(s)
  • Clostridium perfringens, type B, beta toxoid
    18.20
    international unit(s)
    /
    1.00
    millilitre(s)
  • Clostridium perfringens, type C, beta toxoid
    18.20
    international unit(s)
    /
    1.00
    millilitre(s)
  • Clostridium perfringens, type D, epsilon toxoid
    5.30
    international unit(s)
    /
    1.00
    millilitre(s)
  • Clostridium chauvoei, Inactivated
    90.00
    percentage protection
    /
    1.00
    millilitre(s)
  • Clostridium novyi, toxoid
    3.80
    international unit(s)
    /
    1.00
    millilitre(s)
  • Clostridium septicum, toxoid
    4.60
    international unit(s)
    /
    1.00
    millilitre(s)
  • Tetanus toxoid adsorbed
    4.90
    international unit(s)
    /
    1.00
    millilitre(s)
  • Clostridium sordellii, toxoid
    4.40
    international unit(s)
    /
    1.00
    millilitre(s)
  • Clostridium novyi, type D, toxoid
    17.40
    unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AB01
  • QI04AB01
Authorisation status:
  • Surrendered
Authorised in:
  • Belgium
Package description:
  • (ID1): 1 Box with 1 Bottle (Low Density PolyEthylene) with 20 millilitre(s) (20 millilitre(s))
  • (ID2): 1 Box with 1 Bottle (Low Density PolyEthylene) with 50 millilitre(s) (50 millilitre(s))
  • (ID3): 1 Box with 1 Bottle (Low Density PolyEthylene) with 100 millilitre(s) (100 millilitre(s))

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • MSD Animal Health UK Limited
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V329576
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0279/001

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/01/2022
Download
Dutch (PDF)
Published on: 22/03/2022
French (PDF)
Published on: 22/03/2022

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 22/03/2022
French (PDF)
Published on: 22/03/2022
German (PDF)
Published on: 22/03/2022
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."