Veterinary Medicine Information website

EFICUR 50 mg/ml suspension for injection for pigs and cattle

Authorised
  • Ceftiofur hydrochloride
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Product identification

Medicine name:
EFICUR 50 mg/ml suspension for injection for pigs and cattle
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
        8
        day
      • 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:
  • Netherlands
Package description:
  • Type II glass bottle of 50 ml.The bottles are closed with a Type I bromobutyl closure and aluminium capPack size:Cardboard box with 1 glass bottle of 50 ml.
  • Type II glass bottle of 100 ml.The bottles are closed with a Type I bromobutyl closure and aluminium capPack size:Cardboard box with 1 glass bottle of 100 ml.
  • Type II glass bottle of 250 ml.The bottles are closed with a Type I bromobutyl closure and aluminium capThe 250 ml glass bottle has a colourless plastic package as a protective measure in order to avoid glass bottle breaking when itis being used.Pack size:Cardboard box with 1 glass bottle of 250 ml.
  • Type II glass bottles of 100 ml.The bottles are closed with a Type I bromobutyl closure and aluminium capPack size:Cardboard box with 10 glass bottles of 100 ml.
  • Type II glass bottles of 100 ml.The bottles are closed with a Type I bromobutyl closure and aluminium capPack size:Cardboard box with 12 glass bottles of 100 ml.
  • Polyethylene terephthalate (PET) bottle of 50 ml.The bottles are closed with a Type I bromobutyl closure and aluminium capPack size:Cardboard box with 1 PET bottle of 50 ml.
  • Polyethylene terephthalate (PET) bottle of 100 ml.The bottles are closed with a Type I bromobutyl closure and aluminium capPack size:Cardboard box with 1 PET bottle of 100 ml.
  • Polyethylene terephthalate (PET) bottle of 250 ml.The bottles are closed with a Type I bromobutyl closure and aluminium capPack size:Cardboard box with 1 PET bottle of 250 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:
  • Laboratorios Hipra S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Hipra S.A.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 103176
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0190/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 28/09/2025
Download
Dutch (PDF)
Published on: 26/01/2022
Download

Summary of Product Characteristics

English (PDF)
Published on: 28/09/2025
Download