Veterinary Medicine Information website

Prisulfan 200 mg / 40 mg/ml Injektionslösung für Tiere

Authorised
  • Trimethoprim
  • Sulfadiazine
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Product identification

Medicine name:
Prisulfan 200 mg / 40 mg/ml Injektionslösung für Tiere
Active substance:
  • Trimethoprim
  • Sulfadiazine
Target species:
  • Cattle
  • Sheep
  • Horse
  • Pig
  • Dog
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Trimethoprim
    40.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Sulfadiazine
    200.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        12
        day
      • Milk
        5
        day
    • Sheep
      • Meat and offal
        18
        day
      • Milk
        3
        day
    • Horse
      • Meat and offal
        10
        day
    • Pig
      • Meat and offal
        12
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        12
        day
      • Milk
        5
        day
    • Sheep
      • Meat and offal
        18
        day
      • Milk
        3
        day
    • Horse
      • Meat and offal
        10
        day
    • Pig
      • Meat and offal
        12
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01EW10
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories (Ireland) Limited
  • Norbrook Laboratories Limited
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 8-00247
Date of authorisation status change:

Documents

Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 22/01/2026
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Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 22/01/2026
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Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 28/10/2024
Updated on: 22/01/2026
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