Veterinary Medicine Information website

FATROXIMIN, 7.5mg/g, Intrauterinní a vaginální emulze

Authorised
  • Rifaximin

Product identification

Medicine name:
FATROXIMIN, 7.5mg/g, Intrauterinní a vaginální emulze
Active substance:
  • Rifaximin
Target species:
  • Cattle (cow)
  • Horse (mare)
Route of administration:
  • Vaginal use
  • Intrauterine use

Product details

Active substance and strength:
  • Rifaximin
    7.50
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Intrauterine emulsion
Withdrawal period by route of administration:
  • Vaginal use
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Horse (mare)
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
  • Intrauterine use
    • Cattle (cow)
      • Meat and offal
        0
        day
      • Milk
        0
        day
    • Horse (mare)
      • Meat and offal
        no withdrawal period
      • Milk
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QG51AA06
Authorisation status:
  • Valid
Authorised in:
  • Czechia
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
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:
  • 96/843/97-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: 10/06/2025

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 10/06/2025

Labelling

This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 10/06/2025