Veterinary Medicines

Bimoxyvet LA 150 mg/ml, Suspension for Injection for cattle, sheep and pigs

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
Bimoxyvet LA 150 mg/ml, Suspension for Injection for cattle, sheep and pigs
Bimoxyl LA 150 mg/ml injektionsvæske, suspension
Active substance:
  • Amoxicillin trihydrate
Target species:
  • Cattle
  • Sheep
  • Pig
Route of administration:
  • Intramuscular 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
        18
        day
      • Milk
        72
        hour
    • Sheep
      • Meat and offal
        21
        day
    • Pig
      • Meat and offal
        21
        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
Package description:
  • Type I clear, glass vial sealed with a Type I bromobutyl rubber stopper and capped with aluminium overseal.Pack size:Vial of 250 ml
  • Type I clear, glass vial sealed with a Type I bromobutyl rubber stopper and capped with aluminium overseal.Pack size:Vial of 100 ml
  • Clear Polyethylene terephthalate (PET) vials with a Type I chlorobutyl stopper and aluminium cap with plastic flip off sealPack size:Vial of 100 ml
  • Clear Polyethylene terephthalate (PET) vials with a Type I chlorobutyl stopper and aluminium cap with plastic flip off sealPack size:Vial of 250 ml

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:
  • Laboratorios Maymo S.A.U.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Laboratorios Syva S.A.
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 57386
Date of authorisation status change:
Reference member state:
  • Ireland
Procedure number:
  • IE/V/0362/001
Concerned member states:
  • Austria
  • Belgium
  • Denmark
  • Finland
  • France
  • Italy
  • Poland
  • Portugal
  • Romania
  • Spain

Documents

Summary of Product Characteristics

English (PDF)
Published on: 29/09/2024
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Danish (PDF)
Published on: 29/06/2023
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