Veterinary Medicines

EFFIPRO 50 MG SPOT-ON SOLUTION FOR CATS

Authorised
  • Fipronil
Download as PDF

Product identification

Medicine name:
EFFIPRO 50 MG SPOT-ON SOLUTION FOR CATS
Effipro 50 mg διάλυμα για επίχυση σε σημείο (spot-on) για γάτες
Active substance:
  • Fipronil
Target species:
  • Cat
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Fipronil
    50.00
    milligram(s)
    /
    1.00
    Pipette
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:
  • Cyprus
Available in:
  • Cyprus
Package description:
  • Box containing 2 pipettes of 0.5 mL
  • Box containing 3 pipettes of 0.5 mL
  • Box containing 4 pipettes of 0.5 mL
  • Box containing 6 pipettes of 0.5 mL
  • Box containing 8 pipettes of 0.5 mL
  • Box containing 12 pipettes of 0.5 mL
  • Box containing 24 pipettes of 0.5 mL
  • Box containing 30 pipettes of 0.5 mL
  • Box containing 60 pipettes of 0.5 mL
  • Box containing 90 pipettes of 0.5 mL
  • Box containing 150 pipettes of 0.5 mL
  • Box containing 1 blister pack of 1 pipette of 0.5 mL
  • Box containing 2 blister packs of 1 pipette of 0.5 mL
  • Box containing 3 blister packs of 1 pipette of 0.5 mL
  • Box containing 4 blister packs of 1 pipette of 0.5 mL
  • Box containing 6 blister packs of 1 pipette of 0.5 mL
  • Box containing 8 blister packs of 1 pipette of 0.5 mL
  • Box containing 12 blister packs of 1 pipette of 0.5 mL
  • Box containing 24 blister packs of 1 pipette of 0.5 mL
  • Box containing 30 blister packs of 1 pipette of 0.5 mL
  • Box containing 60 blister packs of 1 pipette of 0.5 mL
  • Box containing 90 blister packs of 1 pipette of 0.5 mL
  • Box containing 150 blister packs of 1 pipette of 0.5 mL
  • Box containing 1 pipette of 0.5 mL

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:
  • Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
  • Virbac
Responsible authority:
  • Veterinary Services, Ministry Of Agriculture, Natural Resources And Environment
Authorisation number:
  • CY00185V
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0376/001
Concerned member states:
  • Austria
  • Belgium
  • Bulgaria
  • Cyprus
  • Czechia
  • Denmark
  • Estonia
  • Finland
  • Germany
  • Greece
  • Hungary
  • Ireland
  • Italy
  • Latvia
  • Lithuania
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Slovakia
  • Slovenia
  • Spain
  • Sweden
  • United Kingdom (Northern Ireland)

Documents

Combined File of all Documents

This document does not exist in this language (English). You can find it in another language below.
Greek (PDF)
Published on: 14/10/2024
Download