Coliplus 2,000,000 IU/ml Concentrate for Oral Solution for Use in Drinking Water for Cattle, Sheep,
Coliplus 2,000,000 IU/ml Concentrate for Oral Solution for Use in Drinking Water for Cattle, Sheep,
Not authorised
- COLISTIN SULFATE
Product identification
Medicine name:
Coliplus 2,000,000 IU/ml Concentrate for Oral Solution for Use in Drinking Water for Cattle, Sheep,
Coliplus 2 10*6 IU/ml Oplossing voor gebruik in drinkwater
Coliplus 2 10*6 IU/ml Solution pour administration dans l'eau de boisson
Coliplus 2 10*6 IU/ml Lösung zum Eingeben über das Trinkwasser
Active substance:
- COLISTIN SULFATE
Target species:
-
Pig
-
Cattle (calf)
-
Sheep (lamb)
-
Chicken
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
COLISTIN SULFATE2000000.00/international unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Concentrate for oral solution
Withdrawal period by route of administration:
-
In drinking water use
-
Pig
-
Meat and offal1day
-
-
Cattle (calf)
-
Meat and offal1day
-
Milkno withdrawal periodMeat and offal: 1 day; Milk: Not authorised for use in animals producing milk for human consumption.
-
-
Sheep (lamb)
-
Meat and offal1day
-
Milkno withdrawal periodMeat and offal: 1 day; Milk: Not authorised for use in animals producing milk for human consumption.
-
-
Chicken
-
Meat and offal1day
-
Eggs0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QA07AA10
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Surrendered
Authorised in:
-
Belgium
Package description:
- container of 250 ml
- container of 5 L
- container of 1 L
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:
- Divasa Farmavic S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Divasa Farmavic S.A.
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
- BE-V360184
Date of authorisation status change:
Reference member state:
-
Spain
Procedure number:
- ES/V/0114/001
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Package Leaflet
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Labelling
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