Quinox 6 mg/g oral powder for cattle and sheep
Quinox 6 mg/g oral powder for cattle and sheep
Authorised
- Decoquinate
Product identification
Medicine name:
Quinox 6 mg/g oral powder for cattle and sheep
Active substance:
- Decoquinate
Target species:
-
Cattle
-
Sheep
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Decoquinate6.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Oral powder
Withdrawal period by route of administration:
-
Oral use
-
Cattle
-
Meat and offal0day
-
-
Sheep
-
Meat and offal0day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP51BX04
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Package description:
- Zipped 1 kg heat-sealed bag made of low-density polyethylene/polyamide/aluminium/polyester
- 5 kg heat-sealed bag made of low-density polyethylene/aluminium/polyamide
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Hybrid application – change in strength (Article 19(1)(a) of Regulation (EU) 2019/6)
Marketing authorisation holder:
- HuVepharma
Marketing authorisation date:
Manufacturing sites for batch release:
- Huvepharma S.A.
Responsible authority:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
- CY01030V
Date of authorisation status change:
Reference member state:
-
Ireland
Procedure number:
- IE/V/0599/001
Concerned member states:
-
Belgium
-
Cyprus
-
Czechia
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Netherlands
-
Poland
-
Portugal
-
Slovakia
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Combined File of all Documents
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Greek (PDF)
Published on: 17/08/2026
