FATROXIMIN 100 mg/13,4 g schiuma endouterina per bovine e cavalle non destinate alla produzione di alimenti per il consumo umano
FATROXIMIN 100 mg/13,4 g schiuma endouterina per bovine e cavalle non destinate alla produzione di alimenti per il consumo umano
Authorised
- Rifaximin
Product identification
Medicine name:
FATROXIMIN 100 mg/13,4 g schiuma endouterina per bovine e cavalle non destinate alla produzione di alimenti per il consumo umano
Active substance:
- Rifaximin
Target species:
-
Cattle (cow)
-
Horse (non food-producing)
Route of administration:
-
Intrauterine use
Product details
Active substance and strength:
-
Rifaximin100.00/milligram(s)1.00Cylinder
Pharmaceutical form:
-
Intrauterine foam
Withdrawal period by route of administration:
-
Intrauterine use
- Cattle (cow)
-
Milk0day
-
Meat and offal0day
-
- Horse (non food-producing)
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG51AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Italy
Package description:
- Available only in Italian
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:
- Ministry Of Health
Authorisation number:
- 100077
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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Italian (PDF)
Published on: 12/12/2023
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