T.S.-sol 20/100
  • Sulfametoxazol
  • Trimethoprim
  • Valid
Authorised in these countries:
  • Poland
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Product identification

Medicine name:
T.S.-sol 20/100
Trimsulfasol 20 mg/ml + 100 mg/ml Roztwór do podania w wodzie do picia
Active substance and strength:
  • Sulfametoxazol
  • Trimethoprim
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01EW11
Authorisation number:
  • 2727
Product identification number:
  • 78ad292a-903d-4ec6-ae09-02eb9c1bca99
Permanent identification number:
  • 600000034337

Product details

Legal status of supply:
This information is not available for this product.
Pharmaceutical form:
  • Solution for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Pigs (for fattening)
      • Meat and offal
        8
        day
    • Chicken (broiler)
      • Meat and offal
        5
        day

Availability

Package description:
  • High-density polyethylene bottles with low-density polyethylene screw cap containing 1 litre of product
  • High-density polyethylene jerrycan with high-density polyethylene screw cap containing 5 litres of product
Manufacturing sites for batch release:
  • Dopharma B.V.
Source wholesaler:
This information is not available for this product.
Destination wholesaler:
This information is not available for this product.

Authorisation details

Authorisation status:
  • Valid
Authorisation procedure type:
  • Marketing Authorisation
Procedure number:
  • NL/V/0213/001
Date of authorisation status change:
This information is not available for this product.
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Authorisation country:
  • Poland
Responsible authority:
  • URPL
Marketing authorisation holder:
  • Dopharma Research B.V.
Marketing authorisation issued:
Reference member state:
  • Netherlands
Concerned member states:
  • Belgium
  • Croatia
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Poland
  • Romania
  • Spain
  • United Kingdom (Northern Ireland)
Reference product identifier:
This information is not available for this product.
Source product identifier:
This information is not available for this product.

Additional information

To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet

Documents

Summary of Product Characteristics (PDF)
First published:
Last updated:
Package Leaflet (PDF)
First published:
Last updated:
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