Veterinary Medicines

Betamox LA 150 mg/ml Suspension for Injection

Authorised
  • Amoxicillin trihydrate
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Product identification

Medicine name:
Betamox LA 150 mg/ml Suspension for Injection
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
    172.21
    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:
  • QJ01CA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • The veterinary medicinal product is supplied in 50 ml Type II glass vial sealed with nitryl rubber bung and aluminium overseal OR 50 ml clear polyethylene terephthalate (PET) vial sealed with nitryl rubber bung and aluminium overseal.
  • The veterinary medicinal product is supplied in 100 ml Type II glass vial sealed with nitryl rubber bung and aluminium overseal OR 100 ml clear polyethylene terephthalate (PET) vial sealed with nitryl rubber bung and aluminium overseal.
  • The veterinary medicinal product is supplied in 250 ml clear polyethylene terephthalate (PET) vial sealed with nitryl rubber bung and aluminium overseal.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Norbrook Laboratories (Ireland) Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Norbrook Laboratories Limited
  • Norbrook Manufacturing Limited
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA22664/010/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 26/08/2024
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