Veterinary Medicines

Dexadreson forte 1,32 mg/ml + 2,67 mg/ml Injektionssuspension für Rinder, Pferde und Hunde

Authorised
  • Dexamethasone sodium phosphate
  • DEXAMETHASONE 21-PHENYLPROPIONATE
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Product identification

Medicine name:
Dexadreson forte 1,32 mg/ml + 2,67 mg/ml Injektionssuspension für Rinder, Pferde und Hunde
Active substance:
  • Dexamethasone sodium phosphate
  • DEXAMETHASONE 21-PHENYLPROPIONATE
Target species:
  • Cattle
  • Dog
  • Horse
Route of administration:
  • Periarticular use
  • Subcutaneous use
  • Intramuscular use

Product details

Active substance and strength:
  • Dexamethasone sodium phosphate
    1.32
    milligram(s)
    /
    1.00
    millilitre(s)
  • DEXAMETHASONE 21-PHENYLPROPIONATE
    2.67
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Suspension for injection
Withdrawal period by route of administration:
  • Periarticular use
    • Cattle
      • Milk
        7
        day
      • Meat and offal
        48
        day
    • Dog
    • Horse
      • Milk
        no withdrawal period
      • Meat and offal
        47
        day
  • Subcutaneous use
    • Cattle
      • Milk
        7
        day
      • Meat and offal
        48
        day
    • Dog
    • Horse
      • Milk
        no withdrawal period
      • Meat and offal
        47
        day
  • Intramuscular use
    • Cattle
      • Milk
        7
        day
      • Meat and offal
        48
        day
    • Dog
    • Horse
      • Milk
        no withdrawal period
      • Meat and offal
        47
        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
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis reviewed according to Acquis communautaire
Marketing authorisation holder:
  • Intervet Deutschland GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vet Pharma Friesoythe GmbH
Responsible authority:
  • Federal Office Of Consumer Protection And Food Safety
Authorisation number:
  • 6026382.00.00
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 29/01/2025
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Package Leaflet

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 29/01/2025
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Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
German (PDF)
Published on: 29/01/2025
Download
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