Veterinary Medicines

Cobactan LC, 75 mg, intramammary ointment for lactating cattle

Authorised
  • Cefquinome sulfate
Download as PDF

Product identification

Medicine name:
Cobactan LC, 75 mg, intramammary ointment for lactating cattle
Cobactan LC 75 mg zalf voor intramammair gebruik voor melkgevende runderen
Active substance:
  • Cefquinome sulfate
Target species:
  • Cattle
Route of administration:
  • Intramammary use

Product details

Active substance and strength:
  • Cefquinome sulfate
    88.92
    milligram(s)
    /
    8.00
    gram(s)
Pharmaceutical form:
  • Intramammary ointment
Withdrawal period by route of administration:
  • Intramammary use
    • Cattle
      • Meat and offal
        4
        day
      • Milk
        5
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ51DE90
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • White opaque polyethylene syringes and cleaning towels in paper aluminium copolymer laminate sachet.Packs of 24 syringes and cleaning towels.
  • White opaque polyethylene syringes and cleaning towels in paper aluminium copolymer laminate sachet.Packs of 20 syringes and cleaning towels.
  • White opaque polyethylene syringes and cleaning towels in paper aluminium copolymer laminate sachet.Packs of 15 syringes and cleaning towels.
  • White opaque polyethylene syringes and cleaning towels in paper aluminium copolymer laminate sachet.Packs of 3 syringes and cleaning towels.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Intervet Nederland B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
  • Intervet International GmbH
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 9468
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0467/001
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Lithuania
  • 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.
Dutch (PDF)
Published on: 19/02/2025
Download

Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."