Frontline Combo Line Dog L 100 mg/ml - 90 mg/ml Spot-on oplossing
Frontline Combo Line Dog L 100 mg/ml - 90 mg/ml Spot-on oplossing
Authorised
- Methoprene
- Fipronil
Product identification
Medicine name:
Frontline Combo Line Dog L 100 mg/ml - 90 mg/ml Spot-on oplossing
Frontline Combo Line Dog L 100 mg/ml - 90 mg/ml Solution pour spot-on
Frontline Combo Line Dog L 100 mg/ml - 90 mg/ml Lösung zum Auftropfen
Active substance:
- Methoprene
- Fipronil
Target species:
-
Dog
Route of administration:
-
Spot-on use
Product details
Active substance and strength:
-
Methoprene241.20/milligram(s)2.68millilitre(s)
-
Fipronil268.00/milligram(s)2.68millilitre(s)
Pharmaceutical form:
-
Spot-on solution
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AX65
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Belgium
Available in:
-
Belgium
Package description:
- Frontline Combo Line Dog L 1 Pipette (PE/EVOH/PE/PP/COC/PP/PE/EVOH/PE/ALU/PET) with 2.68 ml Spot-on solution
- Frontline Combo Line Dog L 6 Pipettes (PE/EVOH/PE/PP/COC/PP/PE/EVOH/PE/ALU/PET) with 2.68 ml Spot-on solution
- Frontline Combo Line Dog L 3 Pipettes (PE/EVOH/PE/PP/COC/PP/PE/EVOH/PE/ALU/PET) with 2.68 ml Spot-on solution
- Frontline Combo Line Dog L 6 Pipettes (PANMA/PP/PANMA/ALU/PET) with 2.68 ml Spot-on solution
- Frontline Combo Line Dog L 3 Pipettes (PANMA/PP/PANMA/ALU/PET) with 2.68 ml Spot-on solution
- Frontline Combo Line Dog L 1 Pipette (PANMA/PP/PANMA/ALU/PET) with 2.68 ml Spot-on solution
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Informed Consent application (Article 21 of Regulation (EU) 2019/6)
Marketing authorisation holder:
- Boehringer Ingelheim Animal Health Belgium S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
- Boehringer Ingelheim Animal Health France
Responsible authority:
- Federal Agency For Medicines And Health Products
Authorisation number:
This information is not available for this product.
Date of authorisation status change:
Informed consent reference:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Summary of Product Characteristics
This document does not exist in this language (English). You can find it
in another language below.
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Labelling
This document does not exist in this language (English). You can find it
in another language below.
