Veterinary Medicines

Fatroximin, 300mg, Intrauterinní tableta

Authorised
  • Rifaximin
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Product identification

Medicine name:
Fatroximin, 300mg, Intrauterinní tableta
Active substance:
  • Rifaximin
Target species:
  • Horse (mare)
  • Buffalo (female)
  • Cattle (cow)
Route of administration:
  • Vaginal use
  • Intrauterine use

Product details

Active substance and strength:
  • Rifaximin
    300.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Intrauterine tablet
Withdrawal period by route of administration:
  • Vaginal use
    • Horse (mare)
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Buffalo (female)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
  • Intrauterine use
    • Horse (mare)
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
    • Buffalo (female)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG51AA06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (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:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/841/97-C
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.
Czech (PDF)
Published on: 26/10/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
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