UNI-AMOXICILIN, 510.2mg/g, Premix pro medikaci krmiva
UNI-AMOXICILIN, 510.2mg/g, Premix pro medikaci krmiva
Not authorised
- Amoxicillin
Product identification
Medicine name:
UNI-AMOXICILIN, 510.2mg/g, Premix pro medikaci krmiva
Active substance:
- Amoxicillin
Target species:
-
Pig
-
Chicken (broiler)
Route of administration:
-
In-feed use
Product details
Active substance and strength:
-
Amoxicillin510.20/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Premix for medicated feeding stuff
Withdrawal period by route of administration:
-
In-feed use
-
Pig
-
Meat and offal7day
-
-
Chicken (broiler)
-
Meat and offal1day
-
Eggno withdrawal periodNepoužívat u nosnic, jejichž vejce jsou určena pro lidskou spotřebu.,
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Czechia
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Univit s.r.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Univit s.r.o.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 98/017/07-C
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.
Czech (PDF)
Published on: 26/10/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022
Labelling
This document does not exist in this language (English). You can find it in another language below.
Czech (PDF)
Published on: 26/10/2022