Canaural eyrnadropar, dreifa
Canaural eyrnadropar, dreifa
Authorised
- Prednisolone
- Nystatin
- Framycetin sulfate
- Diethanolamine fusidate
Product identification
Medicine name:
Canaural eyrnadropar, dreifa
Active substance:
- Prednisolone
- Nystatin
- Framycetin sulfate
- Diethanolamine fusidate
Target species:
-
Dog
Route of administration:
-
Auricular use
Product details
Active substance and strength:
-
Prednisolone2.35/milligram(s)1.00millilitre(s)
-
Nystatin94000.00/international unit(s)1.00millilitre(s)
-
Framycetin sulfate4.70/milligram(s)1.00millilitre(s)
-
Diethanolamine fusidate4.70/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Ear drops, suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QS02CA01
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Iceland
Available in:
-
Iceland
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Legal basis not covered by Directive 2001/82/EC
Marketing authorisation holder:
- Dechra Veterinary Products A/S
Marketing authorisation date:
Manufacturing sites for batch release:
- Genera Research Ltd.
- Dales Pharmaceuticals Limited
Responsible authority:
- Icelandic Medicines Agency
Authorisation number:
- 822774
Date of authorisation status change:
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.
Icelandic (PDF)
Published on: 1/03/2022
Package Leaflet
This document does not exist in this language (English). You can find it
in another language below.
Icelandic (PDF)
Published on: 1/03/2022
Updated on: 31/01/2025