Veterinary Medicines

ENGEMYCIN 10% LA, ενέσιμο διάλυμα για βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες

Authorised
  • Oxytetracycline
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Product identification

Medicine name:
ENGEMYCIN 10% LA, ενέσιμο διάλυμα για βοοειδή, πρόβατα, χοίρους, σκύλους και γάτες
Active substance:
  • Oxytetracycline
Target species:
  • Cattle
  • Sheep
  • Pig
  • Dog
  • Cat
Route of administration:
  • Intramuscular and intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Oxytetracycline
    100.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular and intravenous use
    • Cattle
      • Meat and offal
        27
        day
      • Milk
        96
        hour
      • Meat and offal
        18
        day
    • Sheep
      • Meat and offal
        24
        day
      • Milk
        96
        hour
      • Meat and offal
        18
        day
    • Pig
      • Meat and offal
        8
        day
      • Meat and offal
        7
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        27
        day
      • Milk
        96
        hour
      • Meat and offal
        18
        day
    • Sheep
      • Meat and offal
        24
        day
      • Milk
        96
        hour
      • Meat and offal
        18
        day
    • Pig
      • Meat and offal
        8
        day
      • Meat and offal
        7
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Greece
Available in:
  • Greece
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone)
Marketing authorisation holder:
  • Intervet International B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International GmbH
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 65435/14-09-2012/11-02-2013/K-0058202)
Date of authorisation status change: