Sultrim 200 mg/ml + 40 mg/ml Roztwór do wstrzykiwań
Sultrim 200 mg/ml + 40 mg/ml Roztwór do wstrzykiwań
Authorised
- Sulfadoxine
- Trimethoprim
Product identification
Medicine name:
Sultrim 200 mg/ml + 40 mg/ml Roztwór do wstrzykiwań
Active substance:
- Sulfadoxine
- Trimethoprim
Target species:
-
Pig
-
Horse
-
Cattle
Route of administration:
-
Intravenous use
-
Subcutaneous use
-
Intramuscular use
Product details
Active substance and strength:
-
Sulfadoxine200.00milligram(s)1.00millilitre(s)
-
Trimethoprim40.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Withdrawal period by route of administration:
-
Intravenous use
- Pig
-
Meat and offal15day
-
Meat and offal30day
-
Meat and offal6day
-
- Horse
-
Meat and offal6day
-
Meat and offal30day
-
Meat and offal15day
-
- Cattle
-
Meat and offal15day
-
Meat and offal6day
-
Milk4day
-
Meat and offal30day
-
-
Subcutaneous use
- Pig
-
Meat and offal30day
-
Meat and offal6day
-
Meat and offal15day
-
- Horse
-
Meat and offal6day
-
Meat and offal30day
-
Meat and offal15day
-
- Cattle
-
Meat and offal6day
-
Milk4day
-
Meat and offal30day
-
Meat and offal15day
-
-
Intramuscular use
- Pig
-
Meat and offal30day
-
Meat and offal15day
-
Meat and offal6day
-
- Horse
-
Meat and offal6day
-
Meat and offal15day
-
Meat and offal30day
-
- Cattle
-
Meat and offal15day
-
Milk4day
-
Meat and offal6day
-
Meat and offal30day
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW13
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- Available only in Polish
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Biowet Pulawy Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
- Biowet Pulawy Ltd.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2729
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Polish (PDF)
Published on: 4/02/2022
How useful was this page?: