FATROXIMIN 7,5 mg/ g intrauterinná a intravaginálna pena
FATROXIMIN 7,5 mg/ g intrauterinná a intravaginálna pena
Authorised
- Rifaximin
Product identification
Medicine name:
FATROXIMIN 7,5 mg/ g intrauterinná a intravaginálna pena
Active substance:
- Rifaximin
Target species:
-
Cattle (cow)
-
Horse (mare)
Route of administration:
-
Intrauterine use
-
Vaginal use
Product details
Active substance and strength:
-
Rifaximin100.50milligram(s)1.00Container
Pharmaceutical form:
-
Intrauterine foam
Withdrawal period by route of administration:
-
Intrauterine use
-
Cattle (cow)
-
Meat and offal0dayMeat and offal: zero days.
-
Milk0dayMilk: 0 hours.
-
-
Horse (mare)
-
Meat and offal0dayMeat and offal: zero days. Do not use in mares whose meat is intended for human consumption.
-
Milk0dayMilk: zero hours
-
-
-
Vaginal use
-
Cattle (cow)
-
Meat and offal0dayMeat and offal: zero days.
-
Milk0dayMilk: zero hours.
-
-
Horse (mare)
-
Meat and offal0dayMeat and offal: zero days. Do not use in mares whose meat is intended for human consumption.
-
Milk0dayMilk: zero hours.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG51AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Slovakia
Available in:
-
Slovakia
Package description:
- Available only in Slovak
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 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:
- 96/0636/97-S
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Slovak (PDF)
Published on: 14/12/2021
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