Rhemox 500 mg/g powder for use in drinking water for pigs, chicken broilers, duck broilers and turkeys for meat production
Rhemox 500 mg/g powder for use in drinking water for pigs, chicken broilers, duck broilers and turkeys for meat production
Authorised
- Amoxicillin trihydrate
Product identification
Medicine name:
Rhemox 500 mg/g powder for use in drinking water for pigs, chicken broilers, duck broilers and turkeys for meat production
Active substance:
- Amoxicillin trihydrate
Target species:
-
Pig
-
Chicken (broiler)
-
Turkey (for meat production)
-
Duck (broiler)
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Amoxicillin trihydrate500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Pig
-
Meat and offal6day
-
-
Chicken (broiler)
-
Meat and offal1day
-
Eggsno withdrawal periodEggs: Not for use in birds producing or intended to produce eggs for human consumption. Do not use within 4 weeks of the start of the laying period.
-
-
Turkey (for meat production)
-
Meat and offal5day
-
Eggsno withdrawal periodEggs: Not for use in birds producing or intended to produce eggs for human consumption. Do not use within 4 weeks of the start of the laying period.
-
-
Duck (broiler)
-
Meat and offal9day
-
Eggsno withdrawal periodEggs: Not for use in birds producing or intended to produce eggs for human consumption. Do not use within 4 weeks of the start of the laying period.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01CA04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Available in:
-
Greece
Package description:
- sachet of 1 kg
- sachet of 400 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:
- Industrial Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- aniMedica Herstellungs GmbH
- Industria Italiana Integratori Trei S.p.A.
- Industrial Veterinaria S.A.
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 103208/21-10-2020/K-0178002
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0236/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Czechia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
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: 5/04/2023
Greek (PDF)
Published on: 30/10/2025
Labelling
English (PDF)
Download Published on: 27/06/2024
Combined File of all Documents
English (PDF)
Download Published on: 24/07/2025
eu-PUAR-rhemox-500-mg-g-en.pdf
English (PDF)
Download Published on: 5/04/2023
