Veterinary Medicines

Huvacillin 800 mg/g Powder for use in drinking water for chickens and pigs

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
Huvacillin 800 mg/g Powder for use in drinking water for chickens and pigs
HUVACILLIN 800 mg/g prašek za dajanje v vodo za pitje za piščance in prašiče
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Chicken
  • 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
    • Chicken
      • Meat and offal
        1
        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:
  • Slovenia
Package description:
  • Zipped bag of 1kg made of low density polyethylene/aluminium/polyethylene terephthalate.
  • Zipped bag of 500 g made of low density polyethylene/aluminium/polyethylene terephthalate.
  • thermo-sealed sachet of 100 g made of low density polyethylene/aluminium/polyethylene terephthalate
  • Jar of 100 g 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:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
  • Huvepharma S.A.
Responsible authority:
  • Agency For Medicinal Products And Medical Devices Of The Republic Of Slovenia
Authorisation number:
  • DC/V/0758/001
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0365/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 16/07/2024
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Package Leaflet

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Slovenian (PDF)
Published on: 16/07/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Slovenian (PDF)
Published on: 16/07/2024
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