Veterinary Medicines

AMOXICILLIN GLOBAL VET HEALTH 500 mg/g, powder for use in drinking water for chickens, turkeys, ducks and pigs

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
AMOXICILLIN GLOBAL VET HEALTH 500 mg/g, powder for use in drinking water for chickens, turkeys, ducks and pigs
Amoksycylina Global Vet Health 500 mg/g Proszek do podania w wodzie do picia
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Turkey
  • Chicken
  • Duck
  • Pig
Route of administration:
  • Oral 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:
  • Oral use
    • Turkey
      • Meat and offal
        5
        day
    • Chicken
      • Meat and offal
        1
        day
    • Duck
      • Meat and offal
        9
        day
    • Pig
      • Meat and offal
        2
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Poland
Package description:
  • The veterinary medicinal product is packed in thermo-sealed polyethylene / aluminium / polypropylene bags of 100 g.
  • The veterinary medicinal product is packed in thermo-sealed polyethylene / aluminium / polypropylene bags of 200 g.
  • The veterinary medicinal product is packed in thermo-sealed polyethylene / aluminium / polypropylene bags of 500 g.
  • The veterinary medicinal product is packed in thermo-sealed polyethylene / aluminium / polypropylene bags of 1 kg.

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:
  • Global Vet Health S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
  • S P Veterinaria S.A.
Responsible authority:
  • Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
  • 2544
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0350/001
Concerned member states:
  • Bulgaria
  • Cyprus
  • France
  • Greece
  • Italy
  • Malta
  • Poland
  • Portugal
  • Romania
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 13/04/2025
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Polish (PDF)
Published on: 16/03/2022
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 16/03/2022
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 16/03/2022
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