Veterinary Medicines

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

Authorised
  • Sulfamethoxazole
  • Trimethoprim
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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
      • Meat and offal
        6
        day
      • Milk
        96
        hour
    • 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
      • Meat and offal
        6
        day
      • Milk
        96
        hour
    • 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
      • Meat and offal
        6
        day
      • Milk
        96
        hour
    • 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
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:
  • Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Vana Ges.m.b.H.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vana Ges.m.b.H.
Responsible authority:
  • Austrian Agency For Health And Food Safety
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
Updated on: 3/05/2024
Download

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
Updated on: 3/05/2024
Download

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
Updated on: 3/05/2024
Download
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