Veterinary Medicines

INTRADINE-INZ, 300MG\ML ενέσιμο διάλυμα για βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες

Authorised
  • Sulfadimidine sodium
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Product identification

Medicine name:
INTRADINE-INZ, 300MG\ML ενέσιμο διάλυμα για βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες
Active substance:
  • Sulfadimidine sodium
Target species:
  • Cattle
  • Sheep
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Sulfadimidine sodium
    300.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Meat and offal
        16
        day
      • Milk
        156
        hour
    • Sheep
      • Meat and offal
        16
        day
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        40
        day
    • Dog
      • Meat and offal
        no withdrawal period
    • Cat
      • Meat and offal
        no withdrawal period
  • Subcutaneous use
    • Cattle
      • Meat and offal
        16
        day
      • Milk
        156
        hour
    • Sheep
      • Meat and offal
        16
        day
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        40
        day
    • Dog
      • Meat and offal
        no withdrawal period
    • Cat
      • Meat and offal
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01EQ03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Greece
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone)
Marketing authorisation holder:
  • Hellafarm S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories (Ireland) Limited
  • Norbrook Laboratories (Ireland) Limited
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 8802/13-03-1990/K-0033501
Date of authorisation status change: