Veterinary Medicine Information website

Amoxinsol 50 % w/w powder for oral solution

Authorised
  • Amoxicillin
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Product identification

Medicine name:
Amoxinsol 50 % w/w powder for oral solution
Active substance:
  • Amoxicillin
Target species:
  • Turkey
  • Chicken
  • Duck
  • Pig
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Amoxicillin
    43.60
    gram(s)
    /
    100.00
    gram(s)
Pharmaceutical form:
  • Powder for oral solution
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:
  • Ireland
Available in:
  • Ireland
Package description:
  • 150g in foil/polyethylene sachets, 20 sachets packed in a box.
  • 750g in a polyethylene bag sealed with a bag tie in a polypropylene container with polypropylene or polyethylene lid and 100ml measuring scoop.
  • 2.5kg in a polyethylene bag sealed with a bag tie in a polypropylene container with polypropylene or polyethylene lid and 100ml measuring scoop.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Complete application (stand-alone) - Council Directive 81/851/EEC
Marketing authorisation holder:
  • Vetoquinol Ireland Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol UK Limited
  • Vetoquinol Biowet Sp. z o.o.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10983/041/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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