Veterinary Medicine Information website

Belamox 200 mg/ml Pulver und Lösungsmittel zur Herstellung einer Injektionslösung für Rinder, Pferde, Schweine

Authorised
  • Amoxicillin sodium
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Product identification

Medicine name:
Belamox 200 mg/ml Pulver und Lösungsmittel zur Herstellung einer Injektionslösung für Rinder, Pferde, Schweine
Active substance:
  • Amoxicillin sodium
Target species:
  • Cattle
  • Cattle (calf)
  • Horse
  • Pig
Route of administration:
  • Intravenous use
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Amoxicillin sodium
    213.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Powder and solvent for solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Milk
        1
        day
      • Meat and offal
        5
        day
    • Cattle (calf)
      • Meat and offal
        5
        day
    • Horse
      • Milk
        1
        day
      • Meat and offal
        5
        day
  • Subcutaneous use
    • Cattle
      • Meat and offal
        9
        day
      • Milk
        72
        hour
    • Cattle (calf)
      • Meat and offal
        9
        day
    • Horse
      • Meat and offal
        16
        day
      • Milk
        72
        hour
    • Pig
      • Meat and offal
        9
        day
  • Intramuscular use
    • Cattle
      • Meat and offal
        9
        day
      • Milk
        72
        hour
    • Cattle (calf)
      • Meat and offal
        9
        day
    • Horse
      • Meat and offal
        16
        day
      • Milk
        72
        hour
    • Pig
      • Meat and offal
        9
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QJ01CA04
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Germany
Available in:
  • Germany
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Bela-Pharm GmbH & Co. KG
Marketing authorisation date:
Manufacturing sites for batch release:
  • Bela-Pharm GmbH & Co. KG
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 6932991.00.00
Date of authorisation status change:

Documents

Combined File of all Documents

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German (PDF)
Published on: 30/04/2026
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