Benadil, 20mg, Film-coated tablet
Benadil, 20mg, Film-coated tablet
Authorised
- Benazepril hydrochloride
Product identification
Medicine name:
Benadil, 20mg, Film-coated tablet
Benadil, 20mg, Potahovaná tableta
Active substance:
- Benazepril hydrochloride
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Benazepril hydrochloride20.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Film-coated tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QC09AA07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Czechia
Package description:
- Aluminum/Plastic Blister 2 x 14.0 Tablet
- Aluminum/Plastic Blister 7 x 14.0 Tablet
- Aluminium/Aluminium Blister 2 x 14.0 Tablet
- Aluminium/Aluminium Blister 7 x 14.0 Tablet
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:
- Vetviva Richter GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- Vetviva Richter GmbH
Responsible authority:
- Institute For State Control Of Veterinary Biologicals And Medicaments
Authorisation number:
- 96/103/12-C
Date of authorisation status change:
Reference member state:
-
Czechia
Procedure number:
- CZ/V/0111/003
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Denmark
-
France
-
Germany
-
Greece
-
Hungary
-
Luxembourg
-
Netherlands
-
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
eu-puar-czv0111003-mr-benadil-en.pdf
English (PDF)
Download Published on: 14/01/2025
