Veterinary Medicines Information website

OXYTOKEL ενέσιμο διάλυμα 10 IU/ml για άλογα, βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες

Authorised
  • OXYTOCIN SYNTHETIC
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Product identification

Medicine name:
OXYTOKEL ενέσιμο διάλυμα 10 IU/ml για άλογα, βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες
Active substance:
  • OXYTOCIN SYNTHETIC
Target species:
  • Horse
  • Cattle
  • Sheep
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular and intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • OXYTOCIN SYNTHETIC
    10.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular and intravenous use
    • Horse
      • Meat and offal, milk
        0
        day
    • Cattle
      • Meat and offal, milk
        0
        day
    • Sheep
      • Meat and offal, milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Dog
      • Not applicable
        no withdrawal period
    • Cat
      • Not applicable
        no withdrawal period
  • Subcutaneous use
    • Horse
      • Meat and offal, milk
        0
        day
    • Cattle
      • Meat and offal, milk
        0
        day
    • Sheep
      • Meat and offal, milk
        0
        day
    • Pig
      • Meat and offal
        0
        day
    • Dog
      • Not applicable
        no withdrawal period
    • Cat
      • Not applicable
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01BB02
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:
  • Pharmaqua S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Kela Veterinaria
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 22662/14-03-2022//04-05-2022/K-0085201
Date of authorisation status change: