Furosoral10 mg tablets for dogs and cats
Furosoral10 mg tablets for dogs and cats
Authorised
- Furosemide
Product identification
Medicine name:
Furosoral10 mg tablets for dogs and cats
Furosoral Vet. 10 mg tabletter
Active substance:
- Furosemide
Target species:
-
Dog
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Furosemide10.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QC03CA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Package description:
- Cardboard box 3 Aluminium-PVDC/PE/PVC blisters with 10 tablets each, respectively corresponding to 30 tablets per box.
- Cardboard box of 2 Aluminium-PVDC/PE/PVC blisters with 10 tablets each, respectively corresponding to 20 tablets per box.
- Cardboard box of 1 Aluminium-PVDC/PE/PVC blister with 10 tablets each, respectively corresponding to 10 tablets per box.
- Cardboard box of 100 Aluminium-PVDC/PVC blisters with 10 tablets each. Cardboard box containing 10 separate cardboard boxes, each containing 1 blister of 10 tablets.
- Cardboard box of 4 Aluminium-PVDC/PVC blisters with 10 tablets each
- Cardboard box of 10 Aluminium-PVDC/PVC blisters with 10 tablets each. Cardboard box containing 10 separate cardboard boxes, each containing 1 blister of 10 tablets.
- Cardboard box of 6 Aluminium-PVDC/PVC blisters with 10 tablets each
- Cardboard box of 50 Aluminium-PVDC/PVC blisters with 10 tablets each. Cardboard box containing 10 separate cardboard boxes, each containing 1 blister of 10 tablets.
- Cardboard box of 5 Aluminium-PVDC/PVC blisters with 10 tablets each
- Cardboard box of 9 Aluminium-PVDC/PVC blisters with 10 tablets each
- Cardboard box of 8 Aluminium-PVDC/PVC blisters with 10 tablets each
- Cardboard box of 7 Aluminium-PVDC/PVC blisters with 10 tablets each
- Cardboard box of 25 Aluminium-PVDC/PVC blisters with 10 tablets each. Cardboard box containing 10 separate cardboard boxes, each containing 1 blister of 10 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:
- Le Vet. Beheer B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Artesan Pharma GmbH & Co. KG
- Lelypharma B.V.
- Genera d.d.
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 54288
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0192/001
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)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Danish (, TABLETTER 10 MG)
Published on: 15/03/2024
Combined File of all Documents
English (PDF)
Download Published on: 22/01/2024
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