Veterinary Medicines

RHEMOX 500 mg/g

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
RHEMOX 500 mg/g
Rhemox 500 mg/g Pulver zum Eingeben über das Trinkwasser für Schweine, Masthähnchen, Mastenten und Mastputen
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 trihydrate
    500.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Pig
      • Meat and offal
        6
        day
    • Chicken (broiler)
      • Meat and offal
        1
        day
      • Eggs
        no withdrawal period
    • Turkey (for meat production)
      • Meat and offal
        5
        day
      • Eggs
        no withdrawal period
    • Duck (broiler)
      • Meat and offal
        9
        day
      • Eggs
        no withdrawal period
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
  • Medicinal product on medical prescription for non-renewable delivery
Authorisation status:
  • Valid
Authorised in:
  • Austria
Package description:
  • sachet of 1 kg
  • sachet of 400 g
  • sachet of 300 g
  • sachet of 100 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
Responsible authority:
  • Austrian Agency For Health And Food Safety
Authorisation number:
  • 836487
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)

Documents

Labelling

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 28/07/2023
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Package Leaflet

English (PDF)
Published on: 5/04/2023
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German (PDF)
Published on: 28/07/2023
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Summary of Product Characteristics

English (PDF)
Published on: 5/04/2023
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German (PDF)
Published on: 28/07/2023
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eu-PUAR-rhemox-500-mg-g-en.pdf

English (PDF)
Published on: 5/04/2023
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