Cortizeme uz ādas lietojama suspensija suņiem un kaķiem
Cortizeme uz ādas lietojama suspensija suņiem un kaķiem
Authorised
- Prednisolone
- NEOMYCIN SULFATE
Product identification
Medicine name:
Cortizeme uz ādas lietojama suspensija suņiem un kaķiem
Active substance:
- Prednisolone
- NEOMYCIN SULFATE
Target species:
-
Dog
-
Cat
Route of administration:
-
Cutaneous use
Product details
Active substance and strength:
-
Prednisolone1.00/milligram(s)1.00millilitre(s)
-
NEOMYCIN SULFATE5000.00/Infectious unit(s)1.00millilitre(s)
Pharmaceutical form:
-
Cutaneous suspension
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QD07CA03
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Latvia
Available in:
-
Latvia
Package description:
- Available only in Latvian
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Well-established use application (Article 13a of Directive No 2001/82/EC)
Marketing authorisation holder:
- Virbac
Marketing authorisation date:
Manufacturing sites for batch release:
- Virbac
Responsible authority:
- Food And Veterinary Service
Authorisation number:
- V/NRP/00/1230
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
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Published on: 31/07/2025