Veterinary Medicines

PREDNIDERM

Authorised
  • Prednisolone acetate
  • NEOMYCIN SULFATE
Download as PDF

Product identification

Medicine name:
PREDNIDERM
Active substance:
  • Prednisolone acetate
  • NEOMYCIN SULFATE
Target species:
  • Dog
  • Cat
  • Horse
Route of administration:
  • Cutaneous use

Product details

Active substance and strength:
  • Prednisolone acetate
    1.34
    milligram(s)
    /
    1.00
    gram(s)
  • NEOMYCIN SULFATE
    333.33
    international unit(s)
    /
    1.00
    gram(s)
Pharmaceutical form:
  • Cutaneous emulsion
Anatomical therapeutic chemical veterinary (ATCvet) codes:
  • QD07CA01
Legal status of supply:
  • Veterinary medicinal product subject to veterinary prescription
Authorisation status:
  • Valid
Authorised in:
  • Luxembourg
Available in:
  • Luxembourg
Package description:

Additional information

Entitlement type:
  • Marketing Authorisation
Legal basis of product authorisation:
  • Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
  • Vetoquinol S.A.
Marketing authorisation date:
Manufacturing sites for batch release:
  • Vetoquinol S.A.
Responsible authority:
  • Ministry Of Health And Social Security
Authorisation number:
  • V 808/09/07/1232
Date of authorisation status change:

Documents

Summary of Product Characteristics

This document does not exist in this language (English). You can find it in another language below.
French (PDF)
Published on: 20/03/2024
Download