Veterinary Medicines

OXTRA LONG ACTING 200MG/ML, ενέσιμο διάλυμα για βοοειδή, βουβάλια προβατα, αίγες, χοίρους, όρνιθες κρεοπαραγωγής, ινδόρνιθες

Authorised
  • Oxytetracycline
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Product identification

Medicine name:
OXTRA LONG ACTING 200MG/ML, ενέσιμο διάλυμα για βοοειδή, βουβάλια προβατα, αίγες, χοίρους, όρνιθες κρεοπαραγωγής, ινδόρνιθες
Active substance:
  • Oxytetracycline
Target species:
  • Turkey
  • Buffalo
  • Cattle
  • Chicken (broiler)
  • Goat
  • Sheep
  • Pig
Route of administration:
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Oxytetracycline
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Subcutaneous use
    • Turkey
      • Meat and offal
        30
        day
    • Buffalo
      • Meat and offal
        39
        day
      • Milk
        14
        day
    • Cattle
      • Meat and offal
        39
        day
      • Milk
        14
        day
    • Chicken (broiler)
      • Meat and offal
        20
        day
    • Goat
      • Milk
        15
        day
      • Meat and offal
        39
        day
    • Sheep
      • Meat and offal
        26
        day
      • Milk
        15
        day
    • Pig
      • Meat and offal
        16
        day
  • Intramuscular use
    • Turkey
      • Meat and offal
        30
        day
    • Buffalo
      • Meat and offal
        39
        day
      • Milk
        14
        day
    • Cattle
      • Meat and offal
        39
        day
      • Milk
        14
        day
    • Chicken (broiler)
      • Meat and offal
        20
        day
    • Goat
      • Milk
        15
        day
      • Meat and offal
        39
        day
    • Sheep
      • Meat and offal
        26
        day
      • Milk
        15
        day
    • Pig
      • Meat and offal
        16
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Cyprus
Available in:
  • Cyprus
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
Responsible authority:
  • Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
  • 10573
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Greek (PDF)
Published on: 25/08/2022
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