DOXIPULVIS 500 MG/G POWDER FOR USE IN DRINKING WATER / MILK
DOXIPULVIS 500 MG/G POWDER FOR USE IN DRINKING WATER / MILK
Authorised
- Doxycycline hyclate
Product identification
Medicine name:
DOXIPULVIS 500 MG/G POWDER FOR USE IN DRINKING WATER / MILK
Doxipulvis 500 mg/g
Active substance:
- Doxycycline hyclate
Target species:
-
Turkey
-
Pig
-
Cattle (calf)
-
Chicken
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Doxycycline hyclate577.10/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Powder for use in drinking water/milk
Withdrawal period by route of administration:
-
Oral use
-
Turkey
-
Meat and offal12day
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption.
Do not use within 4 weeks before the start of the laying period.
-
-
Pig
-
Meat and offal6day
-
-
Cattle (calf)
-
Meat and offal14day
-
-
Chicken
-
Meat and offal7day
-
Eggsno withdrawal periodNot for use in birds producing eggs for human consumption.
Do not use within 4 weeks before the start of the laying period.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01AA02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Germany
Available in:
-
Germany
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application (Article 13(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- S P Veterinaria S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- S P Veterinaria S.A.
Responsible authority:
- Federal Office Of Consumer Protection And Food Safety
Authorisation number:
- 402241.00.00
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0298/001
Concerned member states:
-
Bulgaria
-
Cyprus
-
Germany
-
Greece
-
Hungary
-
Ireland
-
Italy
-
Malta
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 20/02/2025