DFV DOXIVET 500 mg/g, powder for use in drinking water for pigs and chickens
DFV DOXIVET 500 mg/g, powder for use in drinking water for pigs and chickens
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
DFV DOXIVET 500 mg/g, powder for use in drinking water for pigs and chickens
Active substance:
- Doxycycline hyclate
Target species:
-
Chicken
-
Pig
Route of administration:
-
In drinking water use
Product details
Active substance and strength:
-
Doxycycline hyclate500.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water
Withdrawal period by route of administration:
-
In drinking water use
-
Chicken
-
Meat and offal12day
-
Meat and offal3day
-
-
Pig
-
Meat and offal4day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Package description:
- Bag formed of polyester/aluminium/polyethylene laminate. Bag 2.5 kg
- Bag formed of polyester/aluminium/polyethylene laminate.Carton box 50 x 100 g
- Bag formed of polyester/aluminium/polyethylene laminate.Carton box 250 x 100 g
- Bag formed of polyester/aluminium/polyethylene laminate.Carton box 10 x 100 g
- Bag formed of polyester/aluminium/polyethylene laminate. Bag 1 kg
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-V475306
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0152/002
Concerned member states:
-
Austria
-
Belgium
-
Bulgaria
-
Czechia
-
Denmark
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Lithuania
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Spain
-
Sweden
-
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 and Labelling
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Combined File of all Documents
English (PDF)
Download Published on: 18/12/2025
108007 - par.pdf
English (PDF)
Download Published on: 20/06/2022
Updated on: 21/06/2022