KILTIX ΠΕΡΙΛΑΙΜΙΟ
KILTIX ΠΕΡΙΛΑΙΜΙΟ
Authorised
- Propoxur
- Flumethrin
- Propoxur
- Flumethrin
- Propoxur
- Flumethrin
Product identification
Medicine name:
KILTIX ΠΕΡΙΛΑΙΜΙΟ
Active substance:
- Propoxur
- Flumethrin
- Propoxur
- Flumethrin
- Propoxur
- Flumethrin
Target species:
-
Dog (large)
-
Dog (medium)
-
Dog (small)
Route of administration:
-
Cutaneous use
-
Cutaneous use
-
Cutaneous use
Product details
Active substance and strength:
-
Propoxur4.50gram(s)1.00Collar
-
Flumethrin1.01gram(s)1.00Collar
-
Propoxur3.02gram(s)1.00Collar
-
Flumethrin0.68gram(s)1.00Collar
-
Propoxur1.25gram(s)1.00Collar
-
Flumethrin0.28gram(s)1.00Collar
Pharmaceutical form:
-
Collar
Withdrawal period by route of administration:
-
Cutaneous use
- Dog (large)
-
Not applicableno withdrawal period
-
-
Cutaneous use
- Dog (medium)
-
Not applicableno withdrawal period
-
-
Cutaneous use
- Dog (small)
-
Not applicableno withdrawal period
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53A
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Greece
Available in:
-
Greece
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Complete application (stand-alone)
Marketing authorisation holder:
- Elanco Animal Health GmbH
Marketing authorisation date:
Manufacturing sites for batch release:
- KVP Pharma+Veterinär Produkte GmbH
Responsible authority:
- National Organization For Medicines
Authorisation number:
- 756/09-01-2013/K-0081701
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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