Veterinary Medicines

Cobactan LC, 75 mg, intramammary ointment for lactating cattle

Authorised
  • Cefquinome sulfate
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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 BV
  • 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

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Dutch (PDF)
Published on: 19/02/2025
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Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
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