Veterinary Medicines

DERMIPRED 20 MG TABLETS FOR DOGS

Authorised
  • Prednisolone
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Product identification

Medicine name:
DERMIPRED 20 MG TABLETS FOR DOGS
Dermipred 20 mg tabletten voor honden
Active substance:
  • Prednisolone
Target species:
  • Dog
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Prednisolone
    20.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Withdrawal period by route of administration:
  • Oral use
    • Dog
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH02AB06
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Netherlands
Package description:
  • Cardboard box with 100 tablets
  • Cardboard box with 20 tablets
  • Cardboard box with 100 tablets
  • Cardboard box with 20 tablets

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Hybrid application (Article 13(3) 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 117608
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0301/003
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Germany
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

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Dutch (PDF)
Published on: 28/03/2022
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