Thiafeline 2.5 mg Film-coated Tablets for Cats
Thiafeline 2.5 mg Film-coated Tablets for Cats
Authorised
This information is not available for this product.
Product identification
Medicine name:
Thiafeline 2.5 mg Film-coated Tablets for Cats
Thiafeline vet 2,5 mg Tabletka powlekana
Active substance:
This information is not available for this product.
Target species:
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
This information is not available for this product.
Pharmaceutical form:
-
Film-coated tablet
Withdrawal period by route of administration:
-
Oral use
- Cat
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH03BB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Poland
Package description:
- 300 tablets in a cardboard carton containing 10 aluminium/pvc strips each strip with 30 tablets.
- 150 tablets in a cardboard carton containing 5 aluminium/pvc strips each strip with 30 tablets.
- 120 tablets in a cardboard carton containing 4 aluminium/pvc strips each strip with 30 tablets.
- 60 tablets in a cardboard carton containing 2 aluminium/pvc strips each strip with 30 tablets.
- 30 tablets in a cardboard carton containing 1 aluminium/pvc strips each strip with 30 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:
- Lindopharm GmbH
- Lelypharma B.V.
Responsible authority:
- Office For Registration Of Medicinal Products Medical Devices And Biocidal Products
Authorisation number:
- 2509
Reference member state:
-
Ireland
Procedure number:
- IE/V/0622/001
Concerned member states:
-
Austria
-
Belgium
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Iceland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 11/02/2022
Polish (PDF)
Published on: 4/02/2022
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Polish (PDF)
Published on: 4/02/2022
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