FATROXIMIN 7,5 mg/ml emulsão intra-uterina para bovinos e equinos
FATROXIMIN 7,5 mg/ml emulsão intra-uterina para bovinos e equinos
Authorised
- Rifaximin
Product identification
Medicine name:
FATROXIMIN 7,5 mg/ml emulsão intra-uterina para bovinos e equinos
Active substance:
- Rifaximin
Target species:
-
Cattle
-
Horse
Route of administration:
-
Intrauterine use
Product details
Active substance and strength:
-
Rifaximin7.50milligram(s)1.00gram(s)
Pharmaceutical form:
-
Intrauterine foam
Withdrawal period by route of administration:
-
Intrauterine use
- Cattle
-
Meat and offal0dayCarne e vísceras: zero dias Leite: zero dias
-
Milk0dayCarne e vísceras: zero dias Leite: zero dias
-
- Horse
-
Meat and offal0dayCarne e vísceras: zero dias Leite: zero dias
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG51AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Portugal
Available in:
-
Portugal
Package description:
- Available only in Portuguese
- Available only in Portuguese
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:
- Directorate General For Food And Veterinary
Authorisation number:
- 50871
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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