Veterinary Medicine Information website

Trimazin Forte Vet. granulat 200 + 40 mg/g

Authorised
  • Trimethoprim
  • Sulfadiazine
  • Trimethoprim
  • Sulfadiazine
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Product identification

Medicine name:
Trimazin Forte Vet. granulat 200 + 40 mg/g
Active substance:
  • Trimethoprim
  • Sulfadiazine
  • Trimethoprim
  • Sulfadiazine
Target species:
  • Cattle
  • Pig
  • Horse
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Trimethoprim
    40.00
    milligram(s)
    /
    1.00
    gram(s)
  • Sulfadiazine
    200.00
    milligram(s)
    /
    1.00
    gram(s)
  • Trimethoprim
    40.00
    milligram(s)
    /
    1.00
    gram(s)
  • Sulfadiazine
    200.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Granules
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
    • Pig
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
    • Horse
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
      • Meat and offal
        15
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01EW10
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Scanpharm A/S
Marketing authorisation date:
Manufacturing sites for batch release:
  • Scanpharm A/S
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 12562
Date of authorisation status change: