Tramvetol 50 mg tablets for dogs
Tramvetol 50 mg tablets for dogs
Authorised
- Tramadol hydrochloride
Product identification
Medicine name:
Tramvetol 50 mg tablets for dogs
Tramvetol 50 mg Tablett
Active substance:
- Tramadol hydrochloride
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Tramadol hydrochloride50.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QN02AX02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Sweden
Package description:
- Box of 3 white PVC/PE/PVDC - aluminium blisters of 10 tablets.
- Box of 10 white PVC/PE/PVDC - aluminium blisters of 10 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:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Labiana Pharmaceuticals S.L.U
Responsible authority:
- Swedish Medical Products Agency
Authorisation number:
- 58464
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0267/001
Concerned member states:
-
Austria
-
Belgium
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Latvia
-
Lithuania
-
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
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Swedish (PDF)
Published on: 2/05/2022
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