Veterinary Medicines

Huvamox 800 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:
Huvamox 800 mg/g powder for use in drinking water for chickens, turkeys, ducks and pigs
Huvamox 800 mg/g pulver til anvendelse i drikkevand
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:
  • Denmark
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/ polyethyleneterephthalate/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 S.A.
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 64052
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: 3/05/2024
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Danish (PDF)
Published on: 16/12/2024
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