FLOXACIN 100 mg/ml concentrate for oral solution for chickens and turkeys
FLOXACIN 100 mg/ml concentrate for oral solution for chickens and turkeys
Authorised
- Enrofloxacin
Product identification
Medicine name:
FLOXACIN 100 mg/ml concentrate for oral solution for chickens and turkeys
Floxacin, 100mg/ml, Koncentrát pro perorální roztok
Active substance:
- Enrofloxacin
Target species:
-
Chicken
-
Turkey
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Enrofloxacin100.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Concentrate for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Chicken
-
Meat and offal7dayNot for use in birds producing or intended to produce eggs for human consumption. Do not administer to layer replacement birds within 14 days of coming into lay.
-
-
Turkey
-
Meat and offal13dayNot for use in birds producing or intended to produce eggs for human consumption. Do not administer to layer replacement birds within 14 days of coming into lay.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MA90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Package description:
- 5 litre container: white, high density polyethylene bottles, provided with green screw seal cap of the same material and sealed by induction.
- 1 litre container: white, high density polyethylene bottles, provided with green screw seal cap of the same material and sealed by induction.
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:
- Global Vet Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- S P Veterinaria S.A.
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/094/11-C
Date of authorisation status change:
Reference member state:
-
Portugal
Procedure number:
- PT/V/0103/001
Concerned member states:
-
Bulgaria
-
Cyprus
-
Czechia
-
Hungary
-
Poland
-
Romania
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: 18/05/2023
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 18/05/2023
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Czech (PDF)
Published on: 18/05/2023
