Veterinary Medicines

AMOXYVET 500 mg/g POWDER FOR ORAL SOLUTION

Authorised
  • Amoxicillin
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Product identification

Medicine name:
АМОКСИВЕТ 500 mg/g ПРАХ ЗА ПЕРОРАЛЕН РАЗТВОР
AMOXYVET 500 mg/g POWDER FOR ORAL SOLUTION
Active substance:
  • Amoxicillin
Target species:
  • Cattle
  • Pig
  • Chicken (chick)
Route of administration:
  • In drinking water use

Product details

Active substance and strength:
  • Amoxicillin
    500.00
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Powder for use in drinking water
Withdrawal period by route of administration:
  • In drinking water use
    • Cattle
      • Meat and offal
        1
        day
    • Pig
      • Meat and offal
        7
        day
    • Chicken (chick)
      • Meat and offal
        3
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Bulgaria
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Biovet AD
Marketing authorisation date:
Manufacturing sites for batch release:
  • Biovet J.S.C.
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-2387
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 5/05/2023
Download

Package Leaflet and Labelling

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 5/05/2023
Download
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