Veterinary Medicines Information website

Solamocta 697 mg/g Powder for Use in Drinking Water for Chickens, Ducks and Turkeys

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
Solamocta 697 mg/g Powder for Use in Drinking Water for Chickens, Ducks and Turkeys
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Chicken
  • Turkey
  • Duck
Route of administration:
  • In drinking water use
  • Oral 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
    • Turkey
      • Meat and offal
        5
        day
    • Duck
      • Meat and offal
        9
        day
  • Oral use
    • Chicken
      • Meat and offal
        1
        day
    • Turkey
      • Meat and offal
        5
        day
    • Duck
      • Meat and offal
        9
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Belgium
Available in:
  • Belgium
Package description:
  • 1 kg sachet with outside to inside layers of polyethylene terephthalate, aluminum, polyamide, polyethylene (PET/ALU/PA/PE).
  • 100 g sachet with outside to inside layers of polyethylene terephthalate, aluminum, polyamide, polyethylene (PET/ALU/PA/PE).
  • 1 kg sachet with outside to inside layers of polyethylene terephthalate, polyethylene, aluminum, polyethylene (PET/PE/ALU/PE).
  • 500 g sachet with outside to inside layers of polyethylene terephthalate, polyethylene, aluminum, polyethylene (PET/PE/ALU/PE).
  • 250 g sachet with outside to inside layers of polyethylene terephthalate, aluminum, polyamide, polyethylene (PET/ALU/PA/PE).
  • 100 g sachet with outside to inside layers of polyethylene terephthalate, polyethylene, aluminum, polyethylene (PET/PE/ALU/PE).
  • 500 g sachet with outside to inside layers of polyethylene terephthalate, aluminum, polyamide, polyethylene (PET/ALU/PA/PE).
  • 250 g sachet with outside to inside layers of polyethylene terephthalate, polyethylene, aluminum, polyethylene (PET/PE/ALU/PE).

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:
  • Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Responsible authority:
  • Federal Agency For Medicines And Health Products
Authorisation number:
  • BE-V489502
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0288/001
Concerned member states:
  • Austria
  • Belgium
  • Croatia
  • Czechia
  • Denmark
  • France
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • 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.
French (PDF)
Published on: 13/03/2026
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German (PDF)
Published on: 18/08/2025
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Dutch (PDF)
Published on: 13/03/2026
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Dutch (PDF)
Published on: 18/08/2025
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Labelling

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 18/08/2025
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German (PDF)
Published on: 18/08/2025
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Dutch (PDF)
Published on: 18/08/2025
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