FATROXIMIN 100 mg / 13,4 g intrauterin emulzió szarvasmarhák és lovak részére A.U.V.
FATROXIMIN 100 mg / 13,4 g intrauterin emulzió szarvasmarhák és lovak részére A.U.V.
Authorised
- Rifaximin
Product identification
Medicine name:
FATROXIMIN 100 mg / 13,4 g intrauterin emulzió szarvasmarhák és lovak részére A.U.V.
Active substance:
- Rifaximin
Target species:
-
Cattle
-
Horse
Route of administration:
-
Intrauterine use
Product details
Active substance and strength:
-
Rifaximin7.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Intrauterine suspension
Withdrawal period by route of administration:
-
Intrauterine use
- Cattle
-
Milk0year
-
Meat and offal0day
-
- Horse
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG51AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Hungary
Package description:
- Available only in Hungarian
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:
- Directorate Of Veterinary Medicinal Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Hungarian (PDF)
Published on: 27/02/2024
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Hungarian (PDF)
Published on: 27/02/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Hungarian (PDF)
Published on: 27/02/2024
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