Veterinary Medicine Information website

Diurizone Powder

Not authorised
  • Hydrochlorothiazide
  • Dexamethasone
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Product identification

Medicine name:
Diurizone Powder
Active substance:
  • Hydrochlorothiazide
  • Dexamethasone
Target species:
  • Cattle
  • Horse (non food-producing)
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Hydrochlorothiazide
    75.00
    milligram(s)
    /
    1.00
    gram(s)
  • Dexamethasone
    0.25
    milligram(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Oral powder
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        28
        day
      • Milk
        7
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QC03AX01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Ireland
Package description:
  • 20g polyethylene paper sachet. Twenty sachets per cardboard box.
  • 20g polyethylene paper sachet. Four per cardboard box.

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:
  • Vetoquinol Ireland Limited
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol S.A.
  • Vetoquinol Biowet Sp. z o.o.
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10983/010/001
Date of authorisation status change:

Documents

Summary of Product Characteristics

English (PDF)
Published on: 3/05/2024
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