Fungiconazol 400 mg tablets for dogs
Fungiconazol 400 mg tablets for dogs
Authorised
- Ketoconazole
Product identification
Medicine name:
FUNGICONAZOL 400 MG TABLETS FOR DOGS
Fungiconazol 400 mg tablets for dogs
Active substance:
- Ketoconazole
Target species:
-
Dog
Route of administration:
-
Oral use
Product details
Active substance and strength:
-
Ketoconazole400.00milligram(s)1.00Tablet
Pharmaceutical form:
-
Tablet
Withdrawal period by route of administration:
-
Oral use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QJ02AB02
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Ireland
Package description:
- Cardboard box of 1 Aluminium/PVC/PE/PVDC blister containing 10 tablets each.
- Cardboard box of 10 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
- Cardboard box of 9 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
- Cardboard box of 8 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
- Cardboard box of 7 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
- Cardboard box of 6 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
- Cardboard box of 5 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
- Cardboard box of 4 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
- Cardboard box of 3 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
- Cardboard box of 2 Aluminium/PVC/PE/PVDC blisters containing 10 tablets each.
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:
- Dechra Regulatory B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera d.d.
- Lelypharma B.V.
Responsible authority:
- Health Products Regulatory Authority
Authorisation number:
- VPA22622/047/002
Date of authorisation status change:
Reference member state:
-
France
Procedure number:
- FR/V/0263/002
Concerned member states:
-
Austria
-
Belgium
-
Croatia
-
Czechia
-
Denmark
-
Estonia
-
Finland
-
Greece
-
Hungary
-
Iceland
-
Ireland
-
Italy
-
Latvia
-
Lithuania
-
Luxembourg
-
Netherlands
-
Norway
-
Poland
-
Portugal
-
Romania
-
Slovakia
-
Slovenia
-
Spain
-
Sweden
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
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