Veterinary Medicine Information website

DIACEF 50 mg/ml

Authorised
  • Ceftiofur hydrochloride
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Product identification

Medicine name:
DIACEF 50 mg/ml
Active substance:
  • Ceftiofur hydrochloride
Target species:
  • Pig
  • Cattle
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Ceftiofur hydrochloride
    53.48
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        5
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        6
        day
    • Cattle
      • Milk
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01DD90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Romania
Available in:
  • Romania
Package description:
  • cardboard box containing 1 vial of 250 ml
  • cardboard box containing 1 vial of 100 ml

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:
  • Super's Diana S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Super's Diana S.L.
Responsible authority:
  • Institute For Control Of Biological Products And Veterinary Medicines
Authorisation number:
  • 180089
Date of authorisation status change:
Reference member state:
  • Spain
Procedure number:
  • ES/V/0187/001
Concerned member states:
  • Czechia
  • Hungary
  • Poland
  • Romania

Documents

Package Leaflet

English (PDF)
Published on: 15/10/2025
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Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Romanian (PDF)
Published on: 10/11/2025
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