Veterinary Medicine Information website

Dexamecine 2 mg/ml solution for injection for cattle, horses, pigs, dogs and cats

Authorised
  • Dexamethasone sodium phosphate
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Product identification

Medicine name:
Dexamecine 2 mg/ml solution for injection for cattle, horses, pigs, dogs and cats
Active substance:
  • Dexamethasone sodium phosphate
Target species:
  • Cattle
  • Pig
  • Horse
  • Dog
  • Cat
Route of administration:
  • Intraarticular 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:
  • Intraarticular use
    • Cattle
      • Milk
        72
        hour
      • Meat and offal
        8
        day
    • Pig
      • Meat and offal
        2
        day
    • Horse
      • Meat and offal
        8
        day
  • Intramuscular use
    • Cattle
      • Milk
        72
        hour
      • Meat and offal
        8
        day
    • Pig
      • Meat and offal
        2
        day
    • 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:
  • Netherlands
Package description:
  • 100 ml amber co-ex plastic (polypropylene) vials closed with bromobutyl rubber stoppers and aluminium caps. The bottles are individually packaged in a cardboard box, the package leaflet is enclosed.

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:
  • Vet-Agro Trading Sp. z o.o.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Przedsiebiorstwo Wielobranzowe Vet-Agro Sp. z o.o.
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 120837
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0268/001
Concerned member states:
  • Hungary
  • Italy
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

English (PDF)
Published on: 20/01/2025
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Dutch (PDF)
Published on: 20/01/2025
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