EKYFLOGYL 1.8mg/ml + 8.7mg/ml GEL FOR HORSES
EKYFLOGYL 1.8mg/ml + 8.7mg/ml GEL FOR HORSES
Authorised
- Prednisolone acetate
- Lidocaine hydrochloride monohydrate
Product identification
Medicine name:
EKYFLOGYL 1.8mg/ml + 8.7mg/ml GEL FOR HORSES
Active substance:
- Prednisolone acetate
- Lidocaine hydrochloride monohydrate
Target species:
-
Horse
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Prednisolone acetate2.00/milligram(s)1.00millilitre(s)
-
Lidocaine hydrochloride monohydrate10.70/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Gel
Withdrawal period by route of administration:
-
Cutaneous use
-
Horse
-
Meat and offal10day
-
Milkno withdrawal periodNot authorised for use in animals producing milk for human consumption.
-
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QM02AX99
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Available in:
-
Ireland
Package description:
- Box of one 125 ml Brown Type III glass bottle with a dosing pump made of high-density polyethylene / polypropylene and a dip tube made of low-density polyethylene and polypropylene. Polypropylene screw-fit cap.
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:
- Audevard
Marketing authorisation date:
Manufacturing sites for batch release:
- Dopharma France
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA10481/002/001
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0344/001
Concerned member states:
-
Austria
-
Denmark
-
Finland
-
Germany
-
Ireland
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Sweden
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
