Veterinary Medicines

Oxyvetin, 10 RÜ/ml süstelahus veistele, hobustele, lammastele, kitsedele, sigadele, kassidele ja koertele

Authorised
  • Oxytocin
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Product identification

Medicine name:
Oxyvetin, 10 RÜ/ml süstelahus veistele, hobustele, lammastele, kitsedele, sigadele, kassidele ja koertele
Active substance:
  • Oxytocin
Target species:
  • Horse (mare)
  • Cat (adult female)
  • Goat (adult female)
  • Dog (bitch)
  • Sheep (ewe)
  • Pig (sow)
  • Cattle (cow)
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Oxytocin
    10.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Horse (mare)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Goat (adult female)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep (ewe)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Pig (sow)
      • Meat and offal
        0
        day
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
  • Subcutaneous use
    • Horse (mare)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Goat (adult female)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Sheep (ewe)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Pig (sow)
      • Meat and offal
        0
        day
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01BB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Estonia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Interchemie Werken De Adelaar Eesti AS
Marketing authorisation date:
Manufacturing sites for batch release:
  • Interchemie Werken De Adelaar Eesti AS
Responsible authority:
  • State Agency Of Medicines
Authorisation number:
  • 1122523
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Estonian (PDF)
Published on: 15/11/2023
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