Doxx-Sol 500 mg/g powder for use in drinking water/milk replacer
Doxx-Sol 500 mg/g powder for use in drinking water/milk replacer
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
Doxx-Sol 500 mg/g powder for use in drinking water/milk replacer
Doxx-Sol 500 mg/g Poeder voor toediening in het drinkwater/in de melk
Doxx-Sol 500 mg/g Poudre pour administration dans le lait ou l'eau de boisson
Doxx-Sol 500 mg/g Pulver zum Eingeben über das Trinkwasser/die Milch
Active substance:
- Doxycycline hyclate
Target species:
-
Chicken
-
Cattle (calf)
-
Pig
Route of administration:
-
In drinking water/milk use
Product details
Active substance and strength:
-
Doxycycline hyclate500.00milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
In drinking water/milk use
-
Chicken
-
Meat and offal5day
-
-
Cattle (calf)
-
Meat and offal7day
-
-
Pig
-
Meat and offal8day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Bags of 5 kg formed from polyethylene/aluminium/polyethylene terephtalate laminate.
- Bags of 1 kg formed from polyethylene/aluminium/polyethylene terephtalate laminate.
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:
- BE-V468826
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0185/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Croatia
-
Cyprus
-
Czechia
-
Denmark
-
Estonia
-
France
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Malta
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
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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