File downloaded on 2026-04-22
Source URL: https://medicines.health.europa.eu/veterinary/en/600000046113
Not authorised

Product identification

Medicine name:
DEPOTOCIN 0,07 mg/ml injekčný roztok
Active substance:
  • Carbetocin
Target species:
  • Cattle (cow)
  • Pig (sow)
  • Sheep (ewe)
  • Goat (adult female)
  • Dog (bitch)
Route of administration:
  • Intravenous use
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Carbetocin
    0.07
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle (cow)
      • All relevant tissues
        0
        day
    • Pig (sow)
      • All relevant tissues
        0
        day
    • Sheep (ewe)
      • All relevant tissues
        0
        day
    • Goat (adult female)
      • All relevant tissues
        0
        day
  • Intramuscular use
    • Cattle (cow)
      • All relevant tissues
        0
        day
    • Pig (sow)
      • All relevant tissues
        0
        day
    • Sheep (ewe)
      • All relevant tissues
        0
        day
    • Goat (adult female)
      • All relevant tissues
        0
        day
  • Subcutaneous use
    • Cattle (cow)
      • All relevant tissues
        no withdrawal period
    • Pig (sow)
      • All relevant tissues
        no withdrawal period
    • Sheep (ewe)
      • All relevant tissues
        no withdrawal period
    • Goat (adult female)
      • All relevant tissues
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01BB03
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised 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:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • NORDIC Pharma s.r.o.
Responsible authority:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/415/92-S
Date of authorisation status change:

Documents

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Published on: 18/01/2022
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