Veterinary Medicines

Lodisure 1 mg tablets for cats

Authorised
  • Amlodipine besilate
Download as PDF

Product identification

Medicine name:
Lodisure 1 mg tablets for cats
Lodisure 1 mg compresse per gatti
Active substance:
  • Amlodipine besilate
Target species:
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Amlodipine besilate
    1.40
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Withdrawal period by route of administration:
  • Oral use
    • Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QC08CA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Italy
Package description:
  • Blister made of PVC /aluminium / OPA with a push-through PVC-PVDC/aluminium lidding foil. Each blister contains 14 tablets.1 cardboard carton with 168 tablets.
  • Blister made of PVC /aluminium / OPA with a push-through PVC-PVDC/aluminium lidding foil. Each blister contains 14 tablets.1 cardboard carton with 28 tablets.
  • Blister made of PVC /aluminium / OPA with a push-through PVC-PVDC/aluminium lidding foil. Each blister contains 14 tablets.1 cardboard carton with 84 tablets.
  • Blister made of PVC /aluminium / OPA with a push-through PVC-PVDC/aluminium lidding foil. Each blister contains 14 tablets.1 cardboard carton with 56 tablets.

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
  • Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Lelypharma B.V.
Responsible authority:
  • Ministry Of Health
Authorisation number:
  • 105459
Date of authorisation status change:
Reference member state:
  • Netherlands
Procedure number:
  • NL/V/0339/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Croatia
  • 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

English (PDF)
Published on: 5/10/2023
Updated on: 7/10/2023
Download
Italian (PDF)
Published on: 3/06/2022
Download

Summary of Product Characteristics

English (PDF)
Published on: 20/09/2023
Updated on: 22/09/2023
Download

Package Leaflet and Labelling

English (PDF)
Published on: 20/09/2023
Updated on: 22/09/2023
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."