Tramadog 50 mg tablet for dogs
Tramadog 50 mg tablet for dogs
Authorised
- Tramadol hydrochloride
Product identification
Medicine name:
Tramadog 50 mg tablet for dogs
Tramadol Domes Pharma, 43,9 mg, tabletė šunims
Active substance:
- Tramadol hydrochloride
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Tramadol hydrochloride50.00/milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02AX02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Box with 10 PVC-PVDC / aluminium thermosealed blisters containing 10 tablets each.
- Box with 6 PVC-PVDC / aluminium thermosealed blister containing 10 tablets each.
- Box with 3 PVC-PVDC / aluminium thermosealed blister containing 10 tablets each.
- Box with 1 PVC-PVDC / aluminium thermosealed blister containing 10 tablets each.
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:
- Axience
Marketing authorisation date:
Manufacturing sites for batch release:
- Europeenne De Pharmacotechnie Europhartech
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/22/2704/001-004
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0359/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
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
