COLIPRO 2 000 000 IU/ML CONCENTRATE FOR ORAL SOLUTION FOR PIGS AND POULTRY
COLIPRO 2 000 000 IU/ML CONCENTRATE FOR ORAL SOLUTION FOR PIGS AND POULTRY
Not authorised
- COLISTIN SULFATE
Product identification
Medicine name:
COLIPRO 2 000 000 IU/ML CONCENTRATE FOR ORAL SOLUTION FOR PIGS AND POULTRY
Colivet 2 000 000 IU/ml, Konzentrat für eine orale Lösung für Schweine und Geflügel
Active substance:
- COLISTIN SULFATE
Target species:
-
Poultry
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
COLISTIN SULFATE2.00/million international units1.00millilitre(s)
Pharmaceutical form:
-
Concentrate for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Poultry
-
Meat and offal1day
-
Eggs0day
-
-
Pig
-
Meat and offal1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA10
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Austria
Package description:
- 250 ml high density polyethylene bottle with polypropylene screw cap fitted with a polypropylene dosing device and a polyethylene seal.
- 5 litres high density polyethylene bottle with polypropylene screw cap fitted with a polypropylene dosing device and a polyethylene seal.
- 2 litres high density polyethylene bottle with polypropylene screw cap fitted with a polypropylene dosing device and a polyethylene seal.
- 1 litre high density polyethylene bottle with polypropylene screw cap fitted with a polypropylene dosing device and a polyethylene seal.
- 500 ml high density polyethylene bottle with polypropylene screw cap fitted with a polypropylene dosing device and a polyethylene seal.
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:
- Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
- Ceva Sante Animale
Responsible authority:
- Austrian Agency For Health And Food Safety
Authorisation number:
- 8-00710
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0184/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 11/07/2018
Updated on: 27/06/2025
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 11/07/2018
Updated on: 27/06/2025
Labelling
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 11/07/2018
Updated on: 27/06/2025