Vetrimoxin 50, 50 g/100 g, proszek do sporządzania roztworu doustnego dla świń, bydła, kur i indyków
Vetrimoxin 50, 50 g/100 g, proszek do sporządzania roztworu doustnego dla świń, bydła, kur i indyków
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Vetrimoxin 50, 50 g/100 g, proszek do sporządzania roztworu doustnego dla świń, bydła, kur i indyków
Active substance:
- Amoxicillin trihydrate
Target species:
-
Chicken (hen)
-
Cattle
-
Pig
-
Turkey
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Amoxicillin trihydrate50.00/gram(s)100.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Chicken (hen)
-
Meat and offal2day
-
-
Cattle
-
Meat and offal1day
-
-
Pig
-
Meat and offal7day
-
-
Turkey
-
Meat and offal3day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 1761
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.
Polish (PDF)
Published on: 4/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022