Vitofyllin 50 mg film-coated tablets for dogs
Vitofyllin 50 mg film-coated tablets for dogs
Authorised
- Propentofylline
Product identification
Medicine name:
Vitofyllin 50 mg film-coated tablets for dogs
Vitofyllin 50 mg apvalkotās tabletes suņiem
Active substance:
- Propentofylline
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Propentofylline50.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Film-coated tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QC04AD90
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
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:
- Wirtschaftsgenossenschaft deutscher Tieraerzte eG
Marketing authorisation date:
Manufacturing sites for batch release:
- Artesan Pharma GmbH & Co. KG
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/SRP/23/0014
Date of authorisation status change:
Reference member state:
-
Germany
Procedure number:
- DE/V/0198/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
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
Combined File of all Documents
English (PDF)
Download Published on: 27/09/2022
Updated on: 14/03/2023
Latvian (PDF)
Published on: 9/04/2024
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