Veterinary Medicine Information website

RAPISON 2 mg/ml soluzione iniettabile per bovini, equini, suini

Authorised
  • Dexamethasone
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Product identification

Medicine name:
RAPISON 2 mg/ml soluzione iniettabile per bovini, equini, suini
Active substance:
  • Dexamethasone
Target species:
  • Cattle
  • Horse
  • Pig
Route of administration:
  • Intramuscular use
  • Intravenous use
  • Subcutaneous use
  • Intraarticular use
  • Infiltration

Product details

Active substance and strength:
  • Dexamethasone
    2.00
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Solution for injection
Withdrawal period by route of administration:
  • Intramuscular use
    • Cattle
      • Milk
        60
        hour
      • Meat and offal
        7
        day
    • Horse
      • Meat and offal
        11
        day
    • Pig
      • Meat and offal
        2
        day
  • Intravenous use
    • Cattle
      • Milk
        60
        hour
      • Meat and offal
        7
        day
    • Horse
      • Meat and offal
        11
        day
    • Pig
      • Meat and offal
        2
        day
  • Subcutaneous use
    • Cattle
      • Milk
        60
        hour
      • Meat and offal
        7
        day
    • Horse
      • Meat and offal
        11
        day
    • Pig
      • Meat and offal
        2
        day
  • Intraarticular use
    • Cattle
      • Milk
        60
        hour
      • Meat and offal
        7
        day
    • Horse
      • Meat and offal
        11
        day
    • Pig
      • Meat and offal
        2
        day
  • Infiltration
    • Cattle
      • Milk
        60
        hour
      • Meat and offal
        7
        day
    • Horse
      • Meat and offal
        11
        day
    • Pig
      • Meat and offal
        2
        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:
  • Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Azienda Terapeutica Italiana A.T.I. S.r.l.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Fatro S.p.A.
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: 4/04/2024
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