Veterinary Medicine Information website

GESTAVET OXYTOCIN 10 IU/ml Synthetic Oxytocin, solution for injection

Authorised
  • OXYTOCIN SYNTHETIC

Product identification

Medicine name:
GESTAVET OXYTOCIN 10 IU/ml Synthetic Oxytocin, solution for injection
Active substance:
  • OXYTOCIN SYNTHETIC
Target species:
  • Cattle
  • Dog
  • Sheep
  • Cat
  • Pig
Route of administration:
  • Intramuscular use
  • Intravenous 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 use
    • Cattle
      • Meat and offal
        12
        hour
      • Milk
        12
        hour
    • Sheep
      • Meat and offal
        12
        hour
      • Milk
        12
        hour
    • Pig
      • Meat and offal
        12
        hour
  • Intravenous use
    • Cattle
      • Meat and offal
        12
        hour
      • Milk
        12
        hour
    • Sheep
      • Meat and offal
        12
        hour
      • Milk
        12
        hour
    • Pig
      • Meat and offal
        12
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01BB02
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Package description:
  • The veterinary medicinal product is bottled in sterile 10 ml, colourless Type I glass vial, closed with Type II basic polymeric elastomer closure with anodised aluminium cap. Two 10 ml vials are available in a cardboard box.
  • The veterinary medicinal product is bottled in sterile 50 ml colourless Type II glass vial, closed with Type II basic polymeric elastomer closure with anodised aluminium cap. One vial of 50 ml is available in a cardboard box.
  • The veterinary medicinal product is bottled in sterile 10 ml, colourless Type I glass vial closed with Type II basic polymeric elastomer closure with anodised aluminium cap. Clinical presentation: 25 x 10
  • The veterinary medicinal product is bottled in sterile 10 ml, colourless Type I glass vial closed with Type II basic polymeric elastomer closure with anodised aluminium cap. Clinical presentation: 20 x 10

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Biogenesis Global S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Hipra S.A.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA23501/001/001
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0134/001
Concerned member states:
  • Austria
  • Greece

Documents

Summary of Product Characteristics

English (PDF)
Published on: 28/09/2025
Download

Combined File of all Documents

English (PDF)
Published on: 28/09/2025
Download