Veterinary Medicine Information website

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
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:
  • Slovakia
Available in:
  • Slovakia
Package description:
  • 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.
  • 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 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 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 1 colourless Type II glass vial containing 100 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:
  • Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
  • 96/074/DC/12-S
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

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Slovak (PDF)
Published on: 2/02/2022
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Summary of Product Characteristics

English (PDF)
Published on: 26/10/2025
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