Combotec 67 mg/60.3 mg Spot-on Solution for Small Dogs
Combotec 67 mg/60.3 mg Spot-on Solution for Small Dogs
Authorised
- Fipronil
- Methoprene
Product identification
Medicine name:
Combotec 67 mg/60.3 mg Spot-on Solution for Small Dogs
Combotec 67 mg/60,3 mg spot-on oplossing voor kleine honden
Active substance:
- Fipronil
- Methoprene
Target species:
-
Dog
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Fipronil67.00/milligram(s)0.67millilitre(s)
-
Methoprene60.30/milligram(s)0.67millilitre(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:
-
Netherlands
Available in:
-
Netherlands
Package description:
- A blue pipette is composed of a heat-formed shell and a film. The blue pipette is enclosed in an aluminum blister. 6 pipettes are packed in a cardboard box.
- A blue pipette is composed of a heat-formed shell and a film. The blue pipette is enclosed in an aluminum blister. 2 pipettes are packed in a cardboard box.
- A blue pipette is composed of a heat-formed shell and a film. The blue pipette is enclosed in an aluminum blister. 1 pipette are packed in a cardboard box.
- A blue pipette is composed of a heat-formed shell and a film. The blue pipette is enclosed in an aluminum blister. 4 pipettes are packed in a cardboard box.
- A blue pipette is composed of a heat-formed shell and a film. The blue pipette is enclosed in an aluminum blister. 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.
Responsible authority:
- Medicines Evaluation Board
Authorisation number:
- REG NL 123866
Date of authorisation status change:
Reference member state:
-
Netherlands
Procedure number:
- NL/V/0251/002
Concerned member states:
-
Czechia
-
Hungary
-
Italy
-
Malta
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
