Veterinary Medicines Information website

FLATULEX (17+1,67)MG/ML ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ

Authorised
  • TOCOPHERYL ACETATE
  • SODIUM SELENITE ANHYDROUS
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Product identification

Medicine name:
FLATULEX (17+1,67)MG/ML ΕΝΕΣΙΜΟ ΔΙΑΛΥΜΑ
Active substance:
  • TOCOPHERYL ACETATE
  • SODIUM SELENITE ANHYDROUS
Target species:
  • Pig
  • Horse
  • Cattle
  • Sheep
  • Goat
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • TOCOPHERYL ACETATE
    17.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • SODIUM SELENITE ANHYDROUS
    1.67
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        28
        day
    • Horse
      • Meat and offal
        28
        day
      • Milk
        0
        day
    • Cattle
      • Meat and offal
        28
        day
      • Milk
        0
        day
    • Sheep
      • Meat and offal
        28
        day
      • Milk
        0
        day
    • Goat
      • Meat and offal
        28
        day
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA12CE99
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:
  • PROVET S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • PROVET S.A.
Responsible authority:
  • National Organization For Medicines
Authorisation number:
  • 31805/09-04-2021/K-0018301
Date of authorisation status change: