Frontline Combo Line Cat 100 mg/ml - 120 mg/ml Spot-on oplossing
Frontline Combo Line Cat 100 mg/ml - 120 mg/ml Spot-on oplossing
Authorised
- Methoprene
- Fipronil
Product identification
Medicine name:
Frontline Combo Line Cat 100 mg/ml - 120 mg/ml Spot-on oplossing
Frontline Combo Line Cat 100 mg/ml - 120 mg/ml Solution pour spot-on
Frontline Combo Line Cat 100 mg/ml - 120 mg/ml Lösung zum Auftropfen
Active substance:
- Methoprene
- Fipronil
Target species:
-
Cat
-
Ferret
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Methoprene60.00milligram(s)0.50millilitre(s)
-
Fipronil50.00milligram(s)0.50millilitre(s)
Pharmaceutical form:
-
Spot-on solution
Withdrawal period by route of administration:
-
Cutaneous use
-
Cat
-
Ferret
-
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 Cat 1 Pipette (PE/EVOH/PE/PP/COC/PP/PE/EVOH/PE/ALU/PET) with 0.5 ml Spot-on solution
- Frontline Combo Line Cat 6 Pipettes (PE/EVOH/PE/PP/COC/PP/PE/EVOH/PE/ALU/PET) with 0.5 ml Spot-on solution
- Frontline Combo Line Cat 3 Pipettes (PE/EVOH/PE/PP/COC/PP/PE/EVOH/PE/ALU/PET) with 0.5 ml Spot-on solution
- Frontline Combo Line Cat 6 Pipettes (PANMA/PP/PANMA/ALU/PET) with 0.5 ml Spot-on solution
- Frontline Combo Line Cat 3 Pipettes (PANMA/PP/PANMA/ALU/PET) with 0.5 ml Spot-on solution
- Frontline Combo Line Cat 1 Pipette (PANMA/PP/PANMA/ALU/PET) with 0.5 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 SCS
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
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Package Leaflet
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Labelling
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