Powdox 500 mg/g
Powdox 500 mg/g
Not authorised
- Doxycycline hyclate
Product identification
Medicine name:
Powdox 500 mg/g
Powdox 500 mg/g por ivóvízbe keveréshez sertések, házityúkok és pulykák részére A.U.V.
Active substance:
- Doxycycline hyclate
Target species:
-
Chicken (for reproduction)
-
Chicken (broiler)
-
Pig (for fattening)
-
Turkey (for reproduction)
-
Turkey (for meat production)
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Doxycycline hyclate580.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken (for reproduction)
-
Meat and offal5day
-
Eggsno withdrawal periodEggs: Not authorised for use in laying birds producing eggs for human consumption
-
-
Chicken (broiler)
-
Meat and offal5day
-
Eggsno withdrawal periodEggs: Not authorised for use in laying birds producing eggs for human consumption
-
-
Pig (for fattening)
-
Meat and offal4day
-
-
Turkey (for reproduction)
-
Meat and offal12day
-
Eggsno withdrawal periodEggs: Not authorised for use in laying birds producing eggs for human consumption
-
-
Turkey (for meat production)
-
Meat and offal12day
-
Eggsno withdrawal periodEggs: Not authorised for use in laying birds producing 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:
-
Hungary
Package description:
- bag of 1 kg
- bag of 200 g
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:
- Vetpharma Animal Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Karizoo S.A.
Responsible authority:
- Directorate Of Veterinary Medicinal Products
Authorisation number:
- 3311/X/13 NÉBIH ÁTI
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0177/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
