Veterinary Medicines Information website

Dofatrimject solução injetável

Authorised
  • Sulfadoxine
  • Trimethoprim
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Product identification

Medicine name:
Dofatrimject solução injetável
Active substance:
  • Sulfadoxine
  • Trimethoprim
Target species:
  • Cattle
  • Pig
  • Horse
  • Dog
  • Cat
Route of administration:
  • Intramuscular use
  • Subcutaneous use
  • Intravenous use

Product details

Active substance and strength:
  • Sulfadoxine
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Trimethoprim
    40.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        8
        day
      • Milk
        2
        day
    • Pig
      • Meat and offal
        8
        day
    • Horse
      • Meat and offal
        8
        day
    • Dog
      • Meat and offal
        0
        day
    • Cat
      • Meat and offal
        0
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        8
        day
      • Milk
        2
        day
    • Pig
      • Meat and offal
        8
        day
    • Horse
      • Meat and offal
        8
        day
    • Dog
      • Meat and offal
        0
        day
    • Cat
      • Meat and offal
        0
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        8
        day
      • Milk
        2
        day
    • Pig
      • Meat and offal
        8
        day
    • Horse
      • Meat and offal
        8
        day
    • Dog
      • Meat and offal
        0
        day
    • Cat
      • Meat and offal
        0
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01EW13
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Portugal
Package description:

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:
  • Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Dopharma B.V.
Responsible authority:
  • Directorate General For Food And Veterinary
Authorisation number:
  • 51439
Date of authorisation status change:

Documents

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Published on: 26/12/2022
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