Veterinary Medicines

BLACKLEG VACCINE

Not authorised
  • Clostridium chauvoei, strain 655, cells and equivalent toxoid
  • Clostridium chauvoei, strain 656, cells and equivalent toxoid
  • Clostridium chauvoei, strain 657, cells and equivalent toxoid
  • Clostridium chauvoei, strain 658, cells and equivalent toxoid
  • Clostridium chauvoei, strain 1048, cells and equivalent toxoid
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Product identification

Medicine name:
BLACKLEG VACCINE
Active substance:
  • Clostridium chauvoei, strain 655, cells and equivalent toxoid
  • Clostridium chauvoei, strain 656, cells and equivalent toxoid
  • Clostridium chauvoei, strain 657, cells and equivalent toxoid
  • Clostridium chauvoei, strain 658, cells and equivalent toxoid
  • Clostridium chauvoei, strain 1048, cells and equivalent toxoid
Target species:
  • Cattle
  • Sheep
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Clostridium chauvoei, strain 655, cells and equivalent toxoid
  • Clostridium chauvoei, strain 656, cells and equivalent toxoid
  • Clostridium chauvoei, strain 657, cells and equivalent toxoid
  • Clostridium chauvoei, strain 658, cells and equivalent toxoid
  • Clostridium chauvoei, strain 1048, cells and equivalent toxoid
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Cattle
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI02AB01
  • QI04AB01
Legal status of supply:
  • Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Ireland
Package description:
  • Carton with one low density polyethylene bottle containing 50 ml closed with a butylrubber disc (Intervet UK Ltd) or rubber stopper (Laboratorios Intervet, Salamanca) with aluminium overseal combination cap.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • INTERVET INTERNATIONAL B.V.
Responsible authority:
  • HPRA
Authorisation number:
  • VPA10996/142/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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