DOXINYL, 500 MG/G POWDER FOR USE IN DRINKING WATER FOR PIGS, CHICKENS AND TURKEYS
DOXINYL, 500 MG/G POWDER FOR USE IN DRINKING WATER FOR PIGS, CHICKENS AND TURKEYS
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
LIVIDOXX 500 MG/G ΚΟΝΙΣ ΓΙΑ ΧΟΡΗΓΗΣΗ ΜΕ ΠΟΣΙΜΟ ΝΕΡΟ
DOXINYL, 500 MG/G POWDER FOR USE IN DRINKING WATER FOR PIGS, CHICKENS AND TURKEYS
Active substance:
- Doxycycline hyclate
Target species:
-
Turkey
-
Pig
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Doxycycline hyclate577.00/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
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption. Do not use within 4 weeks before the start of the laying period.
-
-
Pig
-
Meat and offal4day
-
-
Chicken
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption. Do not use within 4 weeks before the start of the laying period.
-
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:
-
Greece
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:
- Industrial Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- aniMedica GmbH
- Industria Italiana Integratori Trei S.p.A.
- Industrial Veterinaria S.A.
- aniMedica Herstellungs GmbH
- aniMedica Herstellungs GmbH
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 42693/27-05-2021/K-0242601
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0406/001
Concerned member states:
-
Austria
-
Czechia
-
Germany
-
Greece
-
Hungary
-
Italy
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Spain
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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in another language below.
Greek (PDF)
Published on: 14/01/2025
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Greek (PDF)
Published on: 14/01/2025
eu-puar-frv0406001-mr-rpe603-en.pdf
English (PDF)
Download Published on: 7/01/2026