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Veterinary Medicines

Multimox pulver og solvens til injektionsvæske, opløsning 212 mg/ml

Authorised
  • Amoxicillin sodium

Product identification

Medicine name:
Multimox 212 mg/ml pulver og solvens til injektionsvæske, opløsning
Multimox pulver og solvens til injektionsvæske, opløsning 212 mg/ml
Active substance:
  • Amoxicillin sodium
Target species:
  • Pig
  • Cattle
Route of administration:
  • Intramuscular use
  • Intravenous use

Product details

Active substance and strength:
  • Amoxicillin sodium
    212.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Powder and solvent for solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Pig
      • Meat and offal
        9
        day
    • Cattle
      • Milk
        3
        day
      • Meat and offal
        9
        day
  • Intravenous use
    • Cattle
      • Meat and offal
        5
        day
      • Milk
        24
        hour
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Authorisation status:
  • Valid
Authorised in:
  • Denmark
Available in:
  • Denmark
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Marketing authorisation holder:
  • Scanvet Animal Health A/S
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bela-Pharm GmbH & Co. KG
Responsible authority:
  • Danish Medicines Agency
Authorisation number:
  • 58257
Date of authorisation status change:

Documents

Summary of Product Characteristics

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Danish (PDF)
Published on: 4/05/2022