Veterinary Medicines

Trymox LA 150 mg/ml Suspension for Injection for Cattle, Sheep, Pigs, Dogs and Cats

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
Trymox LA 150 mg/ml Suspension for Injection for Cattle, Sheep, Pigs, Dogs and Cats
Trymox LA 150 mg/ml инжекционна суспензия за говеда, овце, свине, кучета, котки
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Cattle
  • Dog
  • Sheep
  • Cat
  • Pig
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Amoxicillin trihydrate
    172.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Meat and offal
        39
        day
      • Milk
        108
        hour
    • Dog
    • Sheep
      • Meat and offal
        29
        day
    • Cat
    • Pig
      • Meat and offal
        42
        day
  • Subcutaneous use
    • Dog
    • Cat
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:
  • 50 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. Pack Sizes: 1 x 50 ml vial
  • 100 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. Pack size: 1 x 100 ml vial
  • 250 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. Pack size: 1 x 250 ml vial
  • 50 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. Pack Sizes: 12 x 50 ml vials
  • 100 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. Pack Sizes: 12 x 100 ml vials
  • 250 ml clear, colourless Type II glass vial, closed with nitrile rubber bung and aluminium overseal. Pack Sizes: 6 x 250 ml vials
  • 250 ml clear polyethylene terephthalate vial sealed with nitrile bung and aluminium overseal. Pack size: 1 x 250 ml vial
  • 100 ml clear polyethylene terephthalate vial sealed with nitrile bung and aluminium overseal. Pack size: 1 x 100ml vial
  • 250 ml clear polyethylene terephthalate vial sealed with nitrile bung and aluminium overseal. Pack size: 6 x 250 ml vial
  • 100 ml clear polyethylene terephthalate vial sealed with nitrile bung and aluminium overseal. Pack size: 12 x 100ml vials

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:
  • Univet Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Univet Limited
Responsible authority:
  • Bulgarian Food Safety Authority
Authorisation number:
  • 0022-2876
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0608/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • Cyprus
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Italy
  • Latvia
  • Liechtenstein
  • Lithuania
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 11/02/2022
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Bulgarian (PDF)
Published on: 19/09/2024
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 19/09/2024
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Labelling

This document does not exist in this language (English). You can find it in another language below.
Bulgarian (PDF)
Published on: 19/09/2024
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