Veterinary Medicines

OXYTOCIN VET 10 UI/ml

Authorised
  • Oxytocin
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Product identification

Medicine name:
OXYTOCIN VET 10 UI/ml
Active substance:
  • Oxytocin
Target species:
  • Cattle (cow)
  • Sheep (ewe)
  • Horse (mare)
  • Pig (sow)
  • Goat (adult female)
  • Dog (bitch)
  • Cat (adult female)
Route of administration:
  • Intravenous use
  • 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:
  • Intravenous use
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Sheep (ewe)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Horse (mare)
      • Meat and offal
        0
        day
    • Pig (sow)
      • Meat and offal
        0
        day
    • Goat (adult female)
      • Meat and offal
        0
        day
      • Milk
        0
        day
  • Intramuscular use
    • Cattle (cow)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Sheep (ewe)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Horse (mare)
      • Meat and offal
        0
        day
    • Pig (sow)
      • Meat and offal
        0
        day
    • Dog (bitch)
    • Cat (adult female)
    • Goat (adult female)
      • Milk
        0
        day
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle (cow)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Dog (bitch)
    • Goat (adult female)
      • Milk
        0
        day
      • Meat and offal
        0
        day
    • Cat (adult female)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH01BB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Romania
Available in:
  • Romania
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Directive No 2001/82/EC
Marketing authorisation holder:
  • Veyx Pharma GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Veyx Pharma GmbH
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 160038
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Romanian (PDF)
Published on: 26/10/2021
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