VETMULIN 125 mg/ml Solution for use in drinking water for pigs and chickens
VETMULIN 125 mg/ml Solution for use in drinking water for pigs and chickens
Authorised
- Tiamulin hydrogen fumarate
- Tiamulin hydrogen fumarate
Product identification
Medicine name:
Vetmulin 125 mg/ml opløsning til anvendelse i drikkevand
VETMULIN 125 mg/ml Solution for use in drinking water for pigs and chickens
Active substance:
- Tiamulin hydrogen fumarate
- Tiamulin hydrogen fumarate
Target species:
-
Poultry
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Tiamulin hydrogen fumarate125.00milligram(s)1.00millilitre(s)
-
Tiamulin hydrogen fumarate125.00milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Poultry
-
Eggs0day
-
Eggs0day
-
Meat and offal2day
-
Meat and offal2day
-
-
Pig
-
Meat and offal4day20 mg tiamulinhydrogenfumarat/kg kropsvægt svarende til 16 ml af produktet/100 kg kropsvægt
-
Meat and offal4day20 mg tiamulinhydrogenfumarat/kg kropsvægt svarende til 16 ml af produktet/100 kg kropsvægt
-
Meat and offal2day8,8 mg tiamulinhydrogenfumarat/kg kropsvægt svarende til 7 ml af produktet/100 kg kropsvægt
-
Meat and offal2day8,8 mg tiamulinhydrogenfumarat/kg kropsvægt svarende til 7 ml af produktet/100 kg kropsvægt
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01XQ01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Denmark
Available in:
-
Denmark
Package description:
- 1 litre bottle
- 5 litre jar
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:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Biovet AD
Responsible authority:
- Danish Medicines Agency
Authorisation number:
- 60221
Date of authorisation status change:
Reference member state:
-
Denmark
Procedure number:
- DK/V/0122/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Netherlands
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
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.
Danish (PDF)
Published on: 7/04/2025
PI.pdf
English (PDF)
Download Published on: 27/01/2022
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