Veterinary Medicines

Nelio 5 mg tablet for cats

Authorised
  • Benazepril hydrochloride
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Product identification

Medicine name:
NELIO 5 MG TABLET FOR CATS
Nelio 5 mg tablet for cats
Active substance:
  • Benazepril hydrochloride
Target species:
  • Cat
Route of administration:
  • Oral use

Product details

Active substance and strength:
  • Benazepril hydrochloride
    5.00
    milligram(s)
    /
    1.00
    Tablet
Pharmaceutical form:
  • Tablet
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QC09AA07
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Ireland
Available in:
  • Ireland
Package description:
  • Box with 1 strip (Aluminium/Aluminium) of 10 tablets
  • Box with 50 strips (Aluminium/Aluminium) of 10 tablets
  • Box with 20 strips (Aluminium/Aluminium) of 10 tablets
  • Box with 10 strips (Aluminium/Aluminium) of 10 tablets
  • Box with 5 strips (Aluminium/Aluminium) of 10 tablets
  • Box with 3 strips (Aluminium/Aluminium) of 10 tablets
  • Box with 2 strips (Aluminium/Aluminium) of 10 tablets
  • Box with 1 strip (Polyamide-Aluminium-Desicant/Aluminium) of 10 tablets
  • Box with 2 strips (Polyamide-Aluminium-Desicant/Aluminium) of 10 tablets
  • Box with 3 strips (Polyamide-Aluminium-Desicant/Aluminium) of 10 tablets
  • Box with 5 strips (Polyamide-Aluminium-Desicant/Aluminium) of 10 tablets
  • Box with 10 strips (Polyamide-Aluminium-Desicant/Aluminium) of 10 tablets
  • Box with 20 strips (Polyamide-Aluminium-Desicant/Aluminium) of 10 tablets
  • Box with 50 strips (Polyamide-Aluminium-Desicant/Aluminium) of 10 tablets

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:
  • Ceva Sante Animale
Marketing authorisation date:
Manufacturing sites for batch release:
  • Ceva Sante Animale
Responsible authority:
  • Health Products Regulatory Authority
Authorisation number:
  • VPA10815/031/001
Date of authorisation status change:
Reference member state:
  • France
Procedure number:
  • FR/V/0178/001
Concerned member states:
  • Austria
  • Belgium
  • Czechia
  • Finland
  • Germany
  • Hungary
  • Ireland
  • Italy
  • Luxembourg
  • Netherlands
  • Poland
  • Portugal
  • Romania
  • Spain
  • United Kingdom (Northern Ireland)

Documents

Summary of Product Characteristics

English (PDF)
Published on: 11/01/2024
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