Veterinary Medicines

INTERTOCINE-S 0.018mg/ml ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ

Not authorised
  • Oxytocin acetate
Download as PDF

Product identification

Medicine name:
INTERTOCINE-S 0.018mg/ml ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ
Active substance:
  • Oxytocin acetate
Target species:
  • Horse
  • Cattle
  • Sheep
  • Goat
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular and intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Oxytocin acetate
    0.02
    milligram(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
    • Goat
      • 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
    • Goat
      • 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:
  • Surrendered
Authorised in:
  • Greece
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone)
Marketing authorisation holder:
  • Intervet Hellas A.E.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International GmbH
  • Intervet International B.V.
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 56324/11-08-2010/K-0036101
Date of authorisation status change:
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."