Fatroximin 100 mg/13,4 g putas ievadīšanai dzemdē govīm un ķēvēm
Fatroximin 100 mg/13,4 g putas ievadīšanai dzemdē govīm un ķēvēm
Authorised
- Rifaximin
Product identification
Medicine name:
Fatroximin 100 mg/13,4 g putas ievadīšanai dzemdē govīm un ķēvēm
Active substance:
- Rifaximin
Target species:
-
Cattle (cow)
-
Horse (mare)
Route of administration:
-
Intrauterine use
Product details
Active substance and strength:
-
Rifaximin100.00milligram(s)1.00Vial
Pharmaceutical form:
-
Intrauterine foam
Withdrawal period by route of administration:
-
Intrauterine use
- Cattle (cow)
-
Meat and offal0day
-
Milk0day
-
- Horse (mare)
-
Meat and offal0day
-
Milk0day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QG51AA06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- Available only in Latvian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- PVD
Authorisation number:
- V/NRP/01/1371
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.
Latvian (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.
Latvian (PDF)
Published on: 27/02/2024
Labelling
This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 27/02/2024
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