Veterinary Medicines

Dexatat 2mg/ml

Authorised
  • Dexamethasone sodium phosphate
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Product identification

Medicine name:
Dexatat 2mg/ml
Active substance:
  • Dexamethasone sodium phosphate
Target species:
  • Cattle
  • Dog
  • Horse
  • Cat
  • Pig
Route of administration:
  • Intravenous use
  • Intraarticular use
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Dexamethasone sodium phosphate
    2.63
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intravenous use
    • Cattle
      • Milk
        4
        day
      • Meat and offal
        16
        day
    • Horse
      • Meat and offal
        16
        day
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        4
        day
  • Intraarticular use
    • Cattle
      • Milk
        4
        day
      • Meat and offal
        16
        day
    • Horse
      • Meat and offal
        16
        day
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        4
        day
  • Subcutaneous use
    • Cattle
      • Milk
        4
        day
      • Meat and offal
        16
        day
    • Horse
      • Meat and offal
        16
        day
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        4
        day
  • Intramuscular use
    • Cattle
      • Milk
        4
        day
      • Meat and offal
        16
        day
    • Horse
      • Meat and offal
        16
        day
      • Milk
        no withdrawal period
    • Pig
      • Meat and offal
        4
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH02AB02
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:
  • aniMedica GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • aniMedica GmbH
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 6872823.00.00
Date of authorisation status change:

Documents

Combined File of all Documents

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German (PDF)
Published on: 17/01/2025
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