FLUMEXIL 100 mg/g, granules for use in the drinking water or liquid feed for calves, buffalo calves, foals, lambs, kid-goats, swine and piglets, rabbits, chickens
FLUMEXIL 100 mg/g, granules for use in the drinking water or liquid feed for calves, buffalo calves, foals, lambs, kid-goats, swine and piglets, rabbits, chickens
Authorised
- Flumequine
Product identification
Medicine name:
FLUMEXIL 100 mg/g, granules for use in the drinking water or liquid feed for calves, buffalo calves, foals, lambs, kid-goats, swine and piglets, rabbits, chickens
Active substance:
- Flumequine
Target species:
-
Buffalo
-
Chicken
-
Cattle (calf)
-
Goat
-
Sheep (lamb)
-
Rabbit
-
Pig (piglet)
-
Horse (foal)
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Flumequine100.00/milligram(s)1.00gram(s)
Pharmaceutical form:
-
Granules for oral solution
Withdrawal period by route of administration:
-
Oral use
-
Buffalo
-
Meat and offal8day
-
-
Chicken
-
Meat and offal6dayUse is not permitted in layer hens producing eggs intended for human consumption.
-
-
Cattle (calf)
-
Meat and offal8day
-
-
Goat
-
Meat and offal8day
-
-
Sheep (lamb)
-
Meat and offal8day
-
-
Rabbit
-
Meat and offal6day
-
-
Pig (piglet)
-
Meat and offal8day
-
-
Horse (foal)
-
Meat and offal8day
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ01MB07
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Cyprus
Package description:
- Available only in Greek
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:
- Fatro S.p.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
- 14564
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
English (PDF)
Download Published on: 8/07/2022