Veterinary Medicines

Ceffect 25 mg/ml suspension for injection for cattle and pigs

Authorised
  • Cefquinome sulfate
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Product identification

Medicine name:
Ceffect 25 mg/ml suspension for injection for cattle and pigs
CEFFECT 25 mg/ml Injektionssuspension für Rinder und Schweine
Active substance:
  • Cefquinome sulfate
Target species:
  • Cattle
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Cefquinome sulfate
    29.64
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        5
        day
      • Milk
        24
        hour
    • Pig
      • Meat and offal
        3
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01DE90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
Available in:
  • Austria
Package description:
  • Carton with 1 colourless Type II glass vial containing 100 ml. Each vial is closed with a fluorinatedbromobutyl rubber stopper and sealed with an aluminium cap.
  • Carton with 6 colourless Type II glass vials containing 100 ml. Each vial is closed with a fluorinatedbromobutyl rubber stopper and sealed with an aluminium cap.
  • Carton with 12 colourless Type II glass vials containing 100 ml. Each vial is closed with a fluorinatedbromobutyl rubber stopper and sealed with an aluminium cap.
  • Carton with 1 colourless Type II glass vial containing 250 ml. Each vial is closed with a fluorinatedbromobutyl rubber stopper and sealed with an aluminium cap.
  • Carton with 6 colourless Type II glass vials containing 250 ml. Each vial is closed with a fluorinatedbromobutyl rubber stopper and sealed with an aluminium cap.

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:
  • Emdoka
Marketing authorisation date:
Manufacturing sites for batch release:
  • Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 8-01136
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0470/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • Germany
  • Hungary
  • Italy
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 26/10/2025
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German (PDF)
Published on: 20/05/2019
Updated on: 30/06/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 19/09/2018
Updated on: 30/06/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 19/09/2018
Updated on: 30/06/2025
Download
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