Fiprotec 268 mg Spot on Solution for Large Dogs
Fiprotec 268 mg Spot on Solution for Large Dogs
Authorised
- Fipronil
Product identification
Medicine name:
Fiprotec 268 mg Spot on Solution for Large Dogs
Active substance:
- Fipronil
Target species:
-
Dog
Route of administration:
-
Spot-on use
Product details
Active substance and strength:
-
Fipronil268.00/milligram(s)2.68millilitre(s)
Pharmaceutical form:
-
Spot-on solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AX15
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Lithuania
Package description:
- Blue pipette composed of a heat-formed shell and a film, enclosed in an aluminium blister. 4 pipettes are packed in a cardboard box
- Blue pipette composed of a heat-formed shell and a film, enclosed in an aluminium blister. 6 pipettes are packed in a cardboard box
- Blue pipette composed of a heat-formed shell and a film. 1 pipette is packed in a cardboard box
- Blue pipette composed of a heat-formed shell and a film, enclosed in an aluminium blister. 1 pipette is packed in a cardboard box
- Blue pipette composed of a heat-formed shell and a film, enclosed in an aluminium blister. 2 pipettes are packed in a cardboard box
- Blue pipette composed of a heat-formed shell and a film, enclosed in an aluminium blister. 3 pipettes are packed in a cardboard box
- Blue pipette composed of a heat-formed shell and a film. 6 pipettes are packed in a cardboard box
- Blue pipette composed of a heat-formed shell and a film. 2 pipettes are packed in a cardboard box
- Blue pipette composed of a heat-formed shell and a film. 3 pipettes are packed in a cardboard box
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:
- Beaphar B.V.
Marketing authorisation date:
Manufacturing sites for batch release:
- Beaphar B.V.
- Laboratorios Calier S.A.
Responsible authority:
- State Food And Veterinary Service
Authorisation number:
- LT/2/14/2228/013-017
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0274/004
Concerned member states:
-
Bulgaria
-
Cyprus
-
France
-
Germany
-
Greece
-
Hungary
-
Italy
-
Latvia
-
Lithuania
-
Poland
-
Portugal
-
Romania
-
Spain
-
United Kingdom (Northern Ireland)
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
