Veterinary Medicines

DERMIPRED 10 MG TABLETS FOR DOGS

Not authorised
  • Prednisolone
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Product identification

Medicine name:
DERMIPRED 10 MG TABLETS FOR DOGS
Dermipred 10 mg tabletten voor honden
Active substance:
  • Prednisolone
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Prednisolone
    10.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH02AB06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Surrendered
Authorised in:
  • Netherlands
Package description:
  • Cardboard box with 16 tablets (Aluminium / Polyvinylidene chloride - Thermo elast - Polyvinyl chloride blister)
  • Cardboard box with 96 tablets (Aluminium / Polyvinyl chloride - Aluminium - Polyamide blister)
  • Cardboard box with 16 tablets (Aluminium / Polyvinyl chloride - Aluminium - Polyamide blister)
  • Cardboard box with 96 tablets (Aluminium / Polyvinylidene chloride - Thermo elast - Polyvinyl chloride blister)

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:
  • CEVA Sante Animale B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
Responsible authority:
  • Medicines Evaluation Board
Authorisation number:
  • REG NL 117607
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0301/002

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Dutch (PDF)
Published on: 18/02/2025
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eu-puar-frv0301002-mr-rpe425-en.pdf

English (PDF)
Published on: 7/01/2026
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