T.S.-sol 20/100
-
Sulfametoxazol
-
Trimethoprim
-
Valid
Authorised in these countries:
-
Poland
Page contents
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 offal8day
-
- Chicken (broiler)
-
Meat and offal5day
-
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
First published:
Last updated:
Package Leaflet
(PDF)
First published:
Last updated:
How useful was this page?: