Veterinary Medicines Information website

DIURIZONE POUDRE

Not authorised
  • Hydrochlorothiazide
  • Dexamethasone
Download as PDF

Product identification

Medicine name:
DIURIZONE POUDRE
Active substance:
  • Hydrochlorothiazide
  • Dexamethasone
Target species:
  • Cattle
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:
  • Powder for oral suspension
Withdrawal period by route of administration:
  • Oral use
    • Cattle
      • Meat and offal
        6
        day
      • Milk
        3
        day
    • Cattle
      • Meat and offal
        6
        day
      • Milk
        3
        day
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QC03AX01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • France
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol Biowet Sp. z o.o.
  • Vetoquinol S.A.
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/3978562 4/1992
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.
French (PDF)
Published on: 4/04/2022
Download