Veterinary Medicines

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

Authorised
  • Amoxicillin trihydrate
Download as PDF

Product identification

Medicine name:
AMOXICILLIN GLOBAL VET HEALTH 500 mg/g, powder for use in drinking water for chickens, turkeys, ducks and pigs
AMOXICILLINA GLOBAL VET HEALTH 500 mg/g polvere per uso in acqua da bere per polli, tacchini, anatre e suini
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:
  • Italy
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:
  • Ministry Of Health
Authorisation number:
  • 104848
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: 6/04/2025
Download

Combined File of all Documents

English (PDF)
Published on: 6/04/2025
Download
Italian (PDF)
Published on: 12/04/2022
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."