Doxylin, 433 mg/g, Powder for Use in Drinking Water for Chickens and Turkeys
Doxylin, 433 mg/g, Powder for Use in Drinking Water for Chickens and Turkeys
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
Doxylin, 433 mg/g, Powder for Use in Drinking Water for Chickens and Turkeys
Doxylin 433 mg/g Pulver zum Eingeben über das Trinkwasser für Hühner und Puten
Active substance:
- Doxycycline hyclate
Target species:
-
Turkey
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Doxycycline hyclate500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Turkey
-
Meat and offal12day
-
-
Chicken
-
Meat and offal5day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Package description:
- Securitainer: white polypropylene container, covered with a low density polyethylene cap. The securitainer contains 1 kg of product.
- Bucket: white polypropylene container provided with a polypropylene cap.The bucket contains 5 kg of product
- Bucket: white polypropylene container provided with a polypropylene cap.The bucket contains 2.5 kg of product
- Bucket: white polypropylene container provided with a polypropylene cap.The bucket contains 1 of product.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma B.V.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402122.00.00
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0290/001
Concerned member states:
-
Estonia
-
France
-
Germany
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Poland
-
Portugal
-
Romania
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
English (PDF)
Download Published on: 26/04/2025
Updated on: 25/04/2025
German (PDF)
Published on: 20/05/2025