Skip to main content
Veterinary Medicines

Vanasulf 200 mg/ 40 mg/ml - Injektionslösung für Tiere

Authorised
  • Sulfamethoxazole
  • Trimethoprim

Product identification

Medicine name:
Vanasulf 200 mg/ 40 mg/ml - Injektionslösung für Tiere
Active substance:
  • Sulfamethoxazole
  • Trimethoprim
Target species:
  • Cattle
  • Cattle (pre-ruminant)
  • Dog
  • Horse
  • Cat
  • Pig
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use

Product details

Active substance and strength:
  • Sulfamethoxazole
    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
      • Milk
        96
        hour
      • Meat and offal
        6
        day
    • Cattle (pre-ruminant)
      • Meat and offal
        8
        day
    • Dog
    • Horse
      • Meat and offal
        6
        day
    • Cat
    • Pig
      • Meat and offal
        7
        day
  • Intravenous use
    • Cattle
      • Milk
        96
        hour
      • Meat and offal
        6
        day
    • Cattle (pre-ruminant)
      • Meat and offal
        8
        day
    • Dog
    • Horse
      • Meat and offal
        6
        day
    • Cat
    • Pig
      • Meat and offal
        7
        day
  • Subcutaneous use
    • Cattle
      • Milk
        96
        hour
      • Meat and offal
        6
        day
    • Cattle (pre-ruminant)
      • Meat and offal
        8
        day
    • Dog
    • Horse
      • Meat and offal
        6
        day
    • Cat
    • Pig
      • Meat and offal
        7
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01EW11
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Vana GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vana GmbH
Responsible authority:
  • Austrian Agency For Health And Food Safety Limited
Authorisation number:
  • 8-00017
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: 12/12/2016

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: 29/10/2020

Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 12/12/2016
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."