Fypryst Combo 402 mg/ 361.8 mg spot-on solution for extra large dogs
Fypryst Combo 402 mg/ 361.8 mg spot-on solution for extra large dogs
Authorised
- (S)-Methoprene
- Fipronil
Product identification
Medicine name:
Fypryst Combo 402 mg/ 361.8 mg spot-on solution for extra large dogs
Fypryst Combo 402 mg/ 361,8 mg šķīdums pilināšanai uz ādas ļoti liela auguma suņiem
Active substance:
- (S)-Methoprene
- Fipronil
Target species:
-
Dog
Route of administration:
-
Spot-on use
Product details
Active substance and strength:
-
(S)-Methoprene361.80milligram(s)4.02millilitre(s)
-
Fipronil402.00milligram(s)4.02millilitre(s)
Pharmaceutical form:
-
Spot-on solution
Withdrawal period by route of administration:
-
Spot-on use
-
Dog
-
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QP53AX65
Legal status of supply:
-
Veterinary medicinal product not subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Package description:
- White polypropylene single-dose pipette packaged in aluminium foil sachets. Cardboard box containing 1pipette.
- White polypropylene single-dose pipette packaged in aluminium foil sachets. Cardboard box containing 10 pipettes
- White polypropylene single-dose pipette packaged in aluminium foil sachets. Cardboard box containing 6 pipettes
- White polypropylene single-dose pipette packaged in aluminium foil sachets. Cardboard box containing 3 pipettes.
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Generic application (Article 13(1) of Directive No 2001/82/EC)
Marketing authorisation holder:
- KRKA tovarna zdravil d.d. Novo mesto
Marketing authorisation date:
Manufacturing sites for batch release:
- KRKA tovarna zdravil d.d. Novo mesto
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/DCP/14/0013
Date of authorisation status change:
Reference member state:
-
Hungary
Procedure number:
- HU/V/0133/004/DC
Concerned member states:
-
Bulgaria
-
Croatia
-
Estonia
-
Latvia
-
Lithuania
-
Poland
-
Romania
-
Slovenia
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.
Latvian (PDF)
Published on: 26/03/2024
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 26/03/2024
Labelling
This document does not exist in this language (English). You can find it
in another language below.
Latvian (PDF)
Published on: 26/03/2024
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