Fatroximin 2,94 mg/g uz ādas lietojams aerosols, šķīdums liellopiem, aitām, kazām, cūkām, zirgiem, trušiem, suņiem un kaķiem
Fatroximin 2,94 mg/g uz ādas lietojams aerosols, šķīdums liellopiem, aitām, kazām, cūkām, zirgiem, trušiem, suņiem un kaķiem
Authorised
- Rifaximin
Product identification
Medicine name:
Fatroximin 2,94 mg/g uz ādas lietojams aerosols, šķīdums liellopiem, aitām, kazām, cūkām, zirgiem, trušiem, suņiem un kaķiem
Active substance:
- Rifaximin
Target species:
-
Rabbit
-
Cattle
-
Dog
-
Cat
-
Sheep
-
Goat
-
Horse
-
Pig
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Rifaximin2.94/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Cutaneous spray, solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Rabbit
-
Meat and offal0day
-
-
Cattle
-
Milk0day
-
Meat and offal0day
-
-
Dog
-
Cat
-
Sheep
-
Milk0day
-
Meat and offal0day
-
-
Goat
-
Milk0day
-
Meat and offal0day
-
-
Horse
-
Milk0day
-
Meat and offal0day
-
-
Pig
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD06AX11
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Available in:
-
Latvia
Package description:
- Available only in Latvian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (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:
- Food And Veterinary Service
Authorisation number:
- V/NRP/01/1370
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet and Labelling
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in another language below.
Latvian (PDF)
Published on: 27/05/2025
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