Doxylin 50% WSP
Doxylin 50% WSP
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
Doxylin 50% WSP
Doxylin 50 % WSP 500 mg/g Poeder voor drank
Doxylin 50 % WSP 500 mg/g Poudre pour solution buvable
Doxylin 50 % WSP 500 mg/g Pulver zur Herstellung einer Lösung zum Einnehmen
Active substance:
- Doxycycline hyclate
Target species:
-
Chicken
-
Cattle (calf)
-
Pig
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Doxycycline hyclate500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Chicken
-
Meat and offal5dayNot permitted for use in laying birds producing eggs for human consumption.
-
-
Cattle (calf)
-
Meat and offal7dayNot permitted for use in cattle producing milk for human consumption.
-
-
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:
- Securitainer: white polypropylene container , covered with a low-density polyethylene lid.The securitainer contains 1 kg of product.
- Bucket: white polypropylene bucket provided with a polypropylene lid. The bucket contains 1 kg of product.
- Bucket: white polypropylene bucket provided with a polypropylene lid. The bucket contains 2,5 kg of product.
- Bucket: white polypropylene bucket provided with a polypropylene lid. The bucket contains 5 kg of product.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Dopharma Research B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma B.V.
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:
-
Netherlands
Procedure number:
- NL/V/0171/001
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Cyprus
-
Denmark
-
Estonia
-
Finland
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Sweden
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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