Veterinary Medicine Information website

Vetrimoxin L.A. 150 mg/ml suspension for injection for cattle and pigs

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
Vetrimoxin L.A. 150 mg/ml suspension for injection for cattle and pigs
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Cattle
  • Pig
Route of administration:
  • Intramuscular use

Product details

Active substance and strength:
  • Amoxicillin trihydrate
    172.40
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        3
        day
      • Meat and offal
        18
        day
    • Pig
      • Meat and offal
        16
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Available in:
  • Denmark
Package description:
  • (ID1) 1200 millilitre(s): unspecified outer container with 12 Vial (Plastic) each with 100 millilitre(s)
  • (ID2) 100 millilitre(s): unspecified outer container with 1 Vial (Plastic) with 100 millilitre(s)
  • (ID3) 250 millilitre(s): unspecified outer container with 1 Vial (Plastic) with 250 millilitre(s)
  • (ID4) 3000 millilitre(s): unspecified outer container with 12 Vial (Plastic) each with 250 millilitre(s)

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:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 51404
Date of authorisation status change:
Reference member state:
  • Germany
Procedure number:
  • DE/V/0153/001
Concerned member states:
  • Austria
  • Denmark
  • Finland
  • Iceland
  • Ireland
  • Netherlands
  • Sweden
  • 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.
Danish (, INJEKTIONSVÆSKE, SUSPENSION 150 MG-ML)
Published on: 29/06/2023
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