Tucoprim 125 mg/g - 25 mg/g Prémélange médicamenteux
Tucoprim 125 mg/g - 25 mg/g Prémélange médicamenteux
Not authorised
- Sulfadiazine
- Trimethoprim
Product identification
Medicine name:
Tucoprim 125 mg/g - 25 mg/g Prémélange médicamenteux
Tucoprim 125 mg/g - 25 mg/g Premix voor gemedicineerd voer
Tucoprim 125 mg/g - 25 mg/g Arzneimittel-Vormischung zur Herstellung von Fütterungsarzneimitteln
Active substance:
- Sulfadiazine
- Trimethoprim
Target species:
-
Poultry
-
Pig
Route of administration:
-
In-feed use
Product details
Active substance and strength:
-
Sulfadiazine125.00/milligram(s)1.00gram(s)
-
Trimethoprim25.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Premix for medicated feeding stuff
Withdrawal period by route of administration:
-
In-feed use
-
Poultry
-
Meat and offal24hour
-
Eggno withdrawal periodDo not use in animals producing eggs for human consumption
-
-
Pig
-
Meat and offal5day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01EW10
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Tucoprim 125 mg/g - 25 mg/g - 25 kg PE bag
- Tucoprim 125 mg/g - 25 mg/g - 20 kg PE bag
- Tucoprim 125 mg/g - 25 mg/g - 12 kg PE bag
- Tucoprim 125 mg/g - 25 mg/g - 10 kg PE bag
- Tucoprim 125 mg/g - 25 mg/g - 5 kg PE bag
- Tucoprim 125 mg/g - 25 mg/g - 2 kg PE bag
- Tucoprim 125 mg/g - 25 mg/g - 25 kg paper bag
- Tucoprim 125 mg/g - 25 mg/g - 20 kg paper bag
- Tucoprim 125 mg/g - 25 mg/g - 12 kg paper bag
- Tucoprim 125 mg/g - 25 mg/g - 10 kg paper bag
- Tucoprim 125 mg/g - 25 mg/g - 5 kg paper bag
- Tucoprim 125 mg/g - 25 mg/g - 2 kg paper bag
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - new active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Zoetis Belgium
Marketing authorisation date:
Manufacturing sites for batch release:
- Zoetis Belgium
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
