Benamax Flavour 5 mg tablets for cats and dogs
Benamax Flavour 5 mg tablets for cats and dogs
Authorised
- Benazepril hydrochloride
Product identification
Medicine name:
Benefortin Flavour 5 mg comprimés pour chats et chiens
Benamax Flavour 5 mg tablets for cats and dogs
Active substance:
- Benazepril hydrochloride
Target species:
-
Dog
-
Cat
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Benazepril hydrochloride5.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Cat
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QC09AA07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Luxembourg
Package description:
- PVC/Aluminium/Polyamide blister -forming laminate with aluminium lidding foil with 14 tablets/blister. Cardboard box with 10 blister strips of 14 tablets (140 tablets)
- PVC/Aluminium/Polyamide blister -forming laminate with aluminium lidding foil with 14 tablets/blister. Cardboard box with 4 blister strips of 14 tablets (56 tablets)
- PVC/Aluminium/Polyamide blister -forming laminate with aluminium lidding foil with 14 tablets/blister. Cardboard box with 2 blister strips of 14 tablets (28 tablets)
- PVC/Aluminium/Polyamide blister -forming laminate with aluminium lidding foil with 14 tablets/blister. Cardboard box with 1 blister strip of 14 tablets (14 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:
- Lavet Kft.
Marketing authorisation date:
Manufacturing sites for batch release:
- Lavet Kft.
Responsible authority:
- Ministry Of Health And Social Security
Authorisation number:
- V 993/12/01/2032
Date of authorisation status change:
Reference member state:
-
Hungary
Procedure number:
- HU/V/0113/002
Concerned member states:
-
Austria
-
Belgium
-
Cyprus
-
Czechia
-
France
-
Germany
-
Ireland
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Poland
-
Portugal
-
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.
French (PDF)
Published on: 24/03/2023
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
French (PDF)
Published on: 24/03/2023
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