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Fatroximin 100 mg/13,4 g putas intrauterīnai lietošanai govīm un ķēvēm

Authorised
  • Rifaximin
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Product identification

Medicine name:
Fatroximin 100 mg/13,4 g putas intrauterīnai lietošanai govīm un ķēvēm
Active substance:
  • Rifaximin
Target species:
  • Horse (mare)
  • Cattle (cow)
Route of administration:
  • Intrauterine use

Product details

Active substance and strength:
  • Rifaximin
    100.00
    milligram(s)
    /
    1.00
    Vial
Pharmaceutical form:
  • Intrauterine foam
Withdrawal period by route of administration:
  • Intrauterine use
    • Horse (mare)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Cattle (cow)
      • Milk
        0
        day
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG51AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Latvia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/NRP/01/1371
Date of authorisation status change:

Documents

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Latvian (PDF)
Published on: 12/12/2025
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