Veterinary Medicines

RAPIDEXON

Authorised
  • Dexamethasone sodium phosphate
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Product identification

Medicine name:
RAPIDEXON
Active substance:
  • Dexamethasone sodium phosphate
Target species:
  • Cattle
  • Dog
  • Goat
  • Cat
  • Pig
  • Horse
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Intraarticular 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:
  • Intramuscular use
    • Cattle
      • Milk
        72
        hour
      • Meat and offal
        8
        day
    • Goat
      • Milk
        14
        hour
      • Meat and offal
        60
        day
    • Pig
      • Meat and offal
        2
        day
    • Horse
      • Meat and offal
        8
        day
  • Intravenous use
    • Cattle
      • Milk
        72
        hour
      • Meat and offal
        8
        day
    • Goat
      • Milk
        14
        hour
      • Meat and offal
        60
        day
      • Milk
        14
        hour
      • Meat and offal
        60
        day
    • Goat
      • Milk
        14
        hour
      • Meat and offal
        60
        day
      • Milk
        14
        hour
      • Meat and offal
        60
        day
    • Pig
      • Meat and offal
        2
        day
    • Horse
      • Meat and offal
        8
        day
  • Intraarticular use
    • Horse
      • Meat and offal
        8
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH02AB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Eurovet Animal Health B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Eurovet Animal Health B.V.
Responsible authority:
  • Ministry Of Health
Authorisation number:
This information is not available for this product.
Date of authorisation status change:

Documents

Combined File of all Documents

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Italian (PDF)
Published on: 19/05/2025
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