Veterinary Medicines

Huvamox 800 mg/g powder for use in drinking water for chickens, turkeys, ducks and pigs

Authorised
  • Amoxicillin trihydrate
Download as PDF

Product identification

Medicine name:
Huvamox 800 mg/g powder for use in drinking water for chickens, turkeys, ducks and pigs
HUVAMOX 800 mg/g por ivóvízbe keveréshez házityúkok, pulykák, házi kacsák és sertések számára A.U.V.
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Turkey
  • Chicken
  • Duck
  • Pig
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Amoxicillin trihydrate
    800.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • 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:
  • Hungary
Available in:
  • Hungary
Package description:
  • Zipped 1 kg bag made of low density polyethylene/aluminium/polyethylene terephthalate.
  • Zipped 500 g bag made of low density polyethylene/aluminium/polyethylene terephthalate.
  • Thermo-sealed 100 g bag made of low density polyethylene/aluminium/polyethylene terephthalate.
  • 100 g jar made of high density polyethylene closed with a seal made of low density polyethylene/ polyethylene terephthalate/aluminium and a screw cap made of polypropylene.

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:
  • HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
  • Huvepharma
Responsible authority:
  • Directorate Of Veterinary Medicinal Products
Authorisation number:
  • 4249/X/21 NÉBIH ÁTI
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0642/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Lithuania
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
Download
Hungarian (PDF)
Published on: 1/03/2022
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."