Veterinary Medicine Information website

Arentor DC 250 mg Intramammary Suspension for Dry Cows

Authorised
  • Cefalonium dihydrate
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Product identification

Medicine name:
Arentor DC 250 mg Intramammary Suspension for Dry Cows
Active substance:
  • Cefalonium dihydrate
Target species:
  • Cattle
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • Cefalonium dihydrate
    269.63
    milligram(s)
    /
    1.00
    Syringe
Pharmaceutical form:
  • Intramammary suspension
Withdrawal period by route of administration:
  • Intramammary use
    • Cattle
      • Meat and offal
        21
        day
      • Milk
        96
        hour
      • Milk
        58
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ51DB90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Spain
Package description:
  • A 3g coloured low density polyethylene intramammary syringe with a coloured low density polyethylene dual capPack sizes:Buckets of 120 intramammary syringes and 120 individually wrapped cleaning towelscontaining isopropyl alcohol.
  • A 3g coloured low density polyethylene intramammary syringe with a coloured low density polyethylene dual capPack sizes:Cartons of 20 intramammary syringes and 20 individually wrapped cleaning towels containing isopropyl alcohol.

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:
  • Univet Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Univet Limited
Responsible authority:
  • Spanish Agency Of Medicines And Medical Devices
Authorisation number:
  • 3711 ESP
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0389/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
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English (PDF)
Published on: 30/06/2024
Updated on: 13/03/2026
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Spanish (PDF)
Published on: 30/06/2024
Updated on: 13/03/2026
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 21/06/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 21/06/2024
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