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 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 fumarate125.00/milligram(s)1.00millilitre(s)
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Tiamulin hydrogen fumarate125.00/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
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Poultry
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Meat and offal2day
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Meat and offal2day
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Eggs0day
-
Eggs0day
-
-
Pig
-
Meat and offal2day8,8 mg tiamulinhydrogenfumarat/kg kropsvægt svarende til 7 ml af produktet/100 kg kropsvægt
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Meat and offal2day8,8 mg tiamulinhydrogenfumarat/kg kropsvægt svarende til 7 ml af produktet/100 kg kropsvægt
-
Meat and offal4day20 mg tiamulinhydrogenfumarat/kg kropsvægt svarende til 16 ml af produktet/100 kg kropsvægt
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Meat and offal4day20 mg tiamulinhydrogenfumarat/kg kropsvægt svarende til 16 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:
-
Belgium
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:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Reference member state:
-
Denmark
Procedure number:
- DK/V/0122/001
Concerned member states:
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Austria
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Belgium
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Bulgaria
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Croatia
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Cyprus
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Czechia
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Estonia
-
France
-
Germany
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Greece
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Hungary
-
Ireland
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Italy
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Latvia
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Lithuania
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Netherlands
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Poland
-
Portugal
-
Romania
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Slovakia
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Slovenia
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Spain
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United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
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Package Leaflet
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Labelling
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PI.pdf
English (PDF)
Download Published on: 27/01/2022