Veterinary Medicines

Dexacortone 0,5 mg tablets for dogs and cats

Authorised
  • Dexamethasone
Download as PDF

Product identification

Medicine name:
Dexacortone 0,5 mg tablets for dogs and cats
Dexacortone vet 0,5 mg košļājamās tabletes suņiem un kaķiem
Active substance:
  • Dexamethasone
Target species:
  • Dog
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Dexamethasone
    0.50
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Chewable tablet
Withdrawal period by route of administration:
  • Oral use
    • Dog
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QH02AB02
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Latvia
Package description:
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 2 blisters of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 6 blisters of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 5 blisters of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 1 blister of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 9 blisters of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 4 blisters of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 10 blisters of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 3 blisters of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 8 blisters of 10 tablets.
  • Aluminium - PVC-PE-PVDC blister. Cardboard box of 7 blisters of 10 tablets.

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:
  • Le Vet. Beheer B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Lelypharma B.V.
Responsible authority:
  • Food And Veterinary Service
Authorisation number:
  • V/DCP/17/0051
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0219/001
Concerned member states:
  • Austria
  • Belgium
  • Croatia
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • France
  • Germany
  • Greece
  • Hungary
  • Iceland
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Norway
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Latvian (PDF)
Published on: 17/07/2024
Download
How useful was this page?:
No votes yet
"Please do not include any personal data, such as your name or contact details. If you do, you consent to the processing of that data in accordance with EMA’s Privacy Statement concerning requests for information or access to documents. If you would like a reply from EMA, please Send a question to EMA instead."