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
Cobactan LC, 75 mg, intramammary ointment for lactating cattle
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:
  • Ireland
Available in:
  • Ireland
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 (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Intervet International B.V.
  • Intervet International GmbH
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10996/105/001
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
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

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Published on: 26/01/2022
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