Trimazin 90 % 750 mg/g - 150 mg/g Poeder voor oraal gebruik
Trimazin 90 % 750 mg/g - 150 mg/g Poeder voor oraal gebruik
Authorised
- Trimethoprim
- Sulfadiazine sodium
Product identification
Medicine name:
Trimazin 90 % 750 mg/g - 150 mg/g Poeder voor oraal gebruik
Trimazin 90 % 750 mg/g - 150 mg/g Poudre orale
Trimazin 90 % 750 mg/g - 150 mg/g Pulver zum Einnehmen
Active substance:
- Trimethoprim
- Sulfadiazine sodium
Target species:
-
Pig
Route of administration:
-
In-feed use
-
In drinking water use
Product details
Active substance and strength:
-
Trimethoprim150.00/milligram(s)1.00gram(s)
-
Sulfadiazine sodium815.90/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
In-feed use
-
Pig
-
Meat and offal12day
-
-
-
In drinking water use
-
Pig
-
Meat and offal12day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW10
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Trimazin 90 % 2 kg Bag Oral powder
- Trimazin 90 % 1 kg Bag Oral powder
- Trimazin 90 % 500 g Bag Oral powder
- Trimazin 90 % 100 g Bag Oral powder
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Kela Kempisch Laboratorium Kela Laboratoria
Marketing authorisation date:
Manufacturing sites for batch release:
- KELA Kempisch Laboratorium Kela Laboratoria
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V230036
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
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Package Leaflet
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Labelling
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Package Leaflet and Labelling
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