Emdocolin 50 % Poeder voor toediening in het drinkwater/in de melk
Emdocolin 50 % Poeder voor toediening in het drinkwater/in de melk
Authorised
- COLISTIN SULFATE
Product identification
Medicine name:
Emdocolin 50 % Poeder voor toediening in het drinkwater/in de melk
Active substance:
- COLISTIN SULFATE
Target species:
-
Cattle (pre-ruminant)
-
Pig
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
COLISTIN SULFATE500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Cattle (pre-ruminant)
-
Meat and offal1day
-
-
Pig
-
Meat and offal1day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA10
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Emdocolin 2000 g Bag Powder for use in drinking water/milk
- Emdocolin 1000 g Bag Powder for use in drinking water/milk
- Emdocolin 500 g Bag Powder for use in drinking water/milk
- Emdocolin 100 g Bag Powder for use in drinking water/milk
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Emdoka
Marketing authorisation date:
Manufacturing sites for batch release:
- Lelypharma B.V.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V388997
Date of authorisation status change:
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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