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Dialuene P ενέσιμο εναιώρημα για πρόβατα

Authorised
  • Clostridium chauvoei, toxoid
  • Clostridium novyi, toxoid
  • Immunoglobulins against Clostridium tetani toxin, Equine
  • Clostridium septicum, toxoid
  • Clostridium perfringens, epsilon toxoid
  • Clostridium perfringens, beta toxoid
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Product identification

Medicine name:
Dialuene P ενέσιμο εναιώρημα για πρόβατα
Active substance:
  • Clostridium chauvoei, toxoid
  • Clostridium novyi, toxoid
  • Immunoglobulins against Clostridium tetani toxin, Equine
  • Clostridium septicum, toxoid
  • Clostridium perfringens, epsilon toxoid
  • Clostridium perfringens, beta toxoid
Target species:
  • Sheep
Route of administration:
  • Subcutaneous use

Product details

Active substance and strength:
  • Clostridium chauvoei, toxoid
    0.50
    90% protective dose in guinea pig
    /
    1.00
    millilitre(s)
  • Clostridium novyi, toxoid
    3.50
    international unit(s)
    /
    1.00
    international unit(s)/dose
  • Immunoglobulins against Clostridium tetani toxin, Equine
    2.50
    international unit(s)
    /
    1.00
    international unit(s)/dose
  • Clostridium septicum, toxoid
    2.50
    international unit(s)
    /
    1.00
    international unit(s)/dose
  • Clostridium perfringens, epsilon toxoid
    5.00
    international unit(s)
    /
    1.00
    international unit(s)/dose
  • Clostridium perfringens, beta toxoid
    10.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Emulsion for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Sheep
      • Milk
        0
        day
      • Meat
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QI04AB05
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Cyprus
Available in:
  • Cyprus
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 8(3) of Directive No 2001/83/EC)
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
Responsible authority:
  • Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
  • CY00049V
Date of authorisation status change:

Documents

Combined File of all Documents

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Greek (PDF)
Published on: 16/01/2026
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