Veterinary Medicines

DUPHADERM

Not authorised
  • Hexetidine
  • Prednisolone acetate
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Product identification

Medicine name:
DUPHADERM
Active substance:
  • Hexetidine
  • Prednisolone acetate
Target species:
  • Dog
  • Cat
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Hexetidine
    1.50
    milligram(s)
    /
    1.00
    millilitre(s)
  • Prednisolone acetate
    1.39
    milligram(s)
    /
    1.00
    millilitre(s)
Pharmaceutical form:
  • Cutaneous solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QD07BA01
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:
  • Zoetis France
Marketing authorisation date:
Manufacturing sites for batch release:
  • Zoetis Manufacturing & Research Spain S.L.
Responsible authority:
  • French Agency For Food, Environmental And Occupational Health & Safety
Authorisation number:
  • FR/V/7689822 4/1992
Date of authorisation status change:

Documents

Summary of Product Characteristics

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French (PDF)
Published on: 7/02/2025
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