Altidox 500 mg/g powder for use in drinking water for pigs, chickens and turkeys
Altidox 500 mg/g powder for use in drinking water for pigs, chickens and turkeys
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
Altidox 500 mg/g powder for use in drinking water for pigs, chickens and turkeys
Altidox 500 mg/g Pulver zum Eingeben über das Trinkwasser für Schweine, Hühner und Puten
Active substance:
- Doxycycline hyclate
Target species:
-
Turkey
-
Pig
-
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
-
-
Pig
-
Meat and offal4day
-
-
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
Package description:
- 2 kg bag with an outer layer of polyethylene terephthalate, middle layers of aluminium and polyamide and an inner layer of low density polyethylene (PET/ALU/PA/LDPE).
- 1 kg bag with an outer layer of polyethylene terephthalate, middle layers of aluminium and polyamide and an inner layer of low density polyethylene (PET/ALU/PA/LDPE).
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:
- Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Eurovet Animal Health B.V.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402283.00.00
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0277/001
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
France
-
Germany
-
Hungary
-
Ireland
-
Italy
-
Poland
-
Portugal
-
Spain
-
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: 6/11/2025
German (PDF)
Published on: 20/12/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
German (PDF)
Published on: 20/12/2024
Package Leaflet and Labelling
English (PDF)
Download Published on: 6/11/2025