File downloaded on 2026-04-04
Source URL: https://medicines.health.europa.eu/veterinary/en/600000045800
Authorised

Product identification

Medicine name:
Dermipred 10 mg Tablets for Dogs
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
Authorisation status:
  • Valid
Authorised in:
  • United Kingdom (Northern Ireland)
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
Marketing authorisation holder:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
Responsible authority:
  • The Veterinary Medicines Directorate
Authorisation number:
  • Vm 14966/3079
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0301/002
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)