Veterinary Medicines

Clamoxyl Vet. injektionsvæske, suspension 150 mg/ml

Authorised
  • Amoxicillin trihydrate
  • Amoxicillin trihydrate
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Product identification

Medicine name:
Clamoxyl Vet. 150 mg/ml injektionsvæske, suspension
Clamoxyl Vet. injektionsvæske, suspension 150 mg/ml
Active substance:
  • Amoxicillin trihydrate
  • Amoxicillin trihydrate
Target species:
  • Cattle
  • Pig
  • Cat
  • Sheep
  • Dog
Route of administration:
  • Intramuscular use
  • Subcutaneous use

Product details

Active substance and strength:
  • Amoxicillin trihydrate
    183.00
    milligram(s)
    /
    1.00
    millilitre(s)
  • Amoxicillin trihydrate
    183.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        3
        day
      • Milk
        3
        day
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
    • Pig
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
    • Sheep
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
  • Subcutaneous use
    • Pig
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
    • Sheep
      • Meat and offal
        30
        day
      • Meat and offal
        30
        day
    • Cattle
      • Milk
        3
        day
      • Milk
        3
        day
      • Meat and offal
        30
        day
      • Meat and offal
        30
        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:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Zoetis Animal Health ApS
Marketing authorisation date:
Manufacturing sites for batch release:
  • Haupt Pharma Latina S.r.l.
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 15053
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Danish (, INJEKTIONSVÆSKE, SUSPENSION 150 MG-ML)
Published on: 29/06/2023
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