Veterinary Medicines

PARTOVET 10 IU/ml injekčný roztok

Authorised
  • OXYTOCIN SYNTHETIC
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Product identification

Medicine name:
PARTOVET 10 IU/ml injekčný roztok
Active substance:
  • OXYTOCIN SYNTHETIC
Target species:
  • Cattle (cow)
  • Horse (mare)
  • Pig (sow)
  • Goat (adult female)
  • Sheep (ewe)
  • Dog (bitch)
  • Cat (adult female)
Route of administration:
  • Intramuscular use
  • Subcutaneous 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 (cow)
      • All relevant tissues
        0
        day
    • Horse (mare)
      • All relevant tissues
        0
        day
    • Pig (sow)
      • All relevant tissues
        0
        day
    • Goat (adult female)
      • All relevant tissues
        0
        day
    • Sheep (ewe)
      • All relevant tissues
        0
        day
  • Subcutaneous use
    • Cattle (cow)
      • All relevant tissues
        0
        day
    • Horse (mare)
      • All relevant tissues
        0
        day
    • Pig (sow)
      • All relevant tissues
        0
        day
    • Goat (adult female)
      • All relevant tissues
        0
        day
    • Sheep (ewe)
      • All relevant tissues
        0
        day
  • Intravenous use
    • Cattle (cow)
      • All relevant tissues
        0
        day
    • Horse (mare)
      • All relevant tissues
        0
        day
    • Pig (sow)
      • All relevant tissues
        0
        day
    • Goat (adult female)
      • All relevant tissues
        0
        day
    • Sheep (ewe)
      • All relevant tissues
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01BB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Slovakia
Available in:
  • Slovakia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Divasa Farmavic S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Divasa Farmavic S.A.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/080/04-S
Date of authorisation status change:

Documents

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Published on: 15/07/2025
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