Veterinary Medicines

COLFIVE 5.000.000 UI/ML

Authorised
  • COLISTIN SULFATE
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Product identification

Medicine name:
COLFIVE 5.000.000 UI/ML
Active substance:
  • COLISTIN SULFATE
Target species:
  • Pig
  • Turkey
  • Cattle (calf)
  • Sheep (lamb)
  • Chicken
Route of administration:
  • In drinking water/milk use
  • Oral use

Product details

Active substance and strength:
  • COLISTIN SULFATE
    5000000.00
    international unit(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Concentrate for oral solution
Withdrawal period by route of administration:
  • In drinking water/milk use
    • Pig
      • Meat and offal
        1
        day
    • Turkey
      • Meat and offal
        1
        day
      • Eggs
        0
        day
    • Cattle (calf)
      • Meat and offal
        1
        day
    • Sheep (lamb)
      • Meat and offal
        1
        day
    • Chicken
      • Meat and offal
        1
        day
      • Eggs
        0
        day
  • Oral use
    • Pig
      • Meat and offal
        1
        day
    • Turkey
      • Meat and offal
        1
        day
      • Eggs
        0
        day
    • Cattle (calf)
      • Meat and offal
        1
        day
    • Sheep (lamb)
      • Meat and offal
        1
        day
    • Chicken
      • Meat and offal
        1
        day
      • Eggs
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QA07AA10
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Available in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Industrial Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Industrial Veterinaria S.A.
  • aniMedica GmbH
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 104747
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0221/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Italian (PDF)
Published on: 26/07/2023
Updated on: 27/07/2023
Download

Summary of Product Characteristics

English (PDF)
Published on: 22/12/2023
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Package Leaflet

English (PDF)
Published on: 22/12/2023
Download

Labelling

English (PDF)
Published on: 22/12/2023
Download
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