Soludox 150 mg/g Poudre pour administration dans l’eau de boisson
Soludox 150 mg/g Poudre pour administration dans l’eau de boisson
Not authorised
- Doxycycline hyclate
Product identification
Medicine name:
Soludox 150 mg/g Poudre pour administration dans l’eau de boisson
Soludox 150 mg/g Poeder voor gebruik in drinkwater
Soludox 150 mg/g Pulver zum Eingeben über das Trinkwasser
Active substance:
- Doxycycline hyclate
Target species:
-
Pigeon
-
Pig
-
Ornamental bird
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Doxycycline hyclate150.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Pigeon
-
Meat and offalno withdrawal periodDo not use in animals intended for human consumption
-
-
Pig
-
Meat and offal12day12 days after cessation of the treatment
-
-
Ornamental bird
-
Chicken
-
Meat and offal9day9 days after cessation of the treatment
-
Eggno withdrawal periodDo not use in animals laying eggs for human consumption
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- Soludox 150 mg/g 1 container (PE) of 100 g
- Soludox 150 mg/g 1 container (PE) of 500 g
- Soludox 150 mg/g 1 container (PE) of 1000 g
- Soludox 150 mg/g 1 bag (PE) of 1000 g
- Soludox 150 mg/g 10 sachet (PE/ALU) of 100 g
- Soludox 150 mg/g 1 sachet (PE/ALU) of 100 g
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - known active substance (Article 8 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Dechra Veterinary Products
Marketing authorisation date:
Manufacturing sites for batch release:
- Dechra Veterinary Products
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
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