KARIDOX 500 mg/g
KARIDOX 500 mg/g
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
KARIDOX 500 mg/g
Karidox 500 mg/g Proszek do podania w wodzie do picia
Active substance:
- Doxycycline hyclate
Target species:
-
Chicken (for reproduction)
-
Chicken (broiler)
-
Pigs (for fattening)
-
Turkey (for reproduction)
-
Turkey (for meat production)
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Doxycycline hyclate580.00milligram(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 birds producing eggs for human consumption
-
- Chicken (broiler)
-
Meat and offal5day
-
Eggsno withdrawal periodEggs: Not authorised for use in birds producing eggs for human consumption
-
- Pigs (for fattening)
-
Meat and offal4day
-
- Turkey (for reproduction)
-
Meat and offal12day
-
Eggsno withdrawal periodEggs: Not authorised for use in birds producing eggs for human consumption
-
- Turkey (for meat production)
-
Meat and offal12day
-
Eggsno withdrawal periodEggs: Not authorised for use in 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:
-
Valid
Authorised in:
-
Poland
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:
- Laboratorios Karizoo S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Laboratorios Karizoo S.A.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2256
Reference member state:
-
Spain
Procedure number:
- ES/V/0178/001
Concerned member states:
-
Germany
-
Hungary
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 6/04/2023
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