PREDNISOLONA FATRO 25 mg/ml SOLUCION INYECTABLE
PREDNISOLONA FATRO 25 mg/ml SOLUCION INYECTABLE
Authorised
- Prednisolone sodium phosphate
Product identification
Medicine name:
PREDNISOLONA FATRO 25 mg/ml SOLUCION INYECTABLE
Active substance:
- Prednisolone sodium phosphate
Target species:
-
Dog
-
Cat
Route of administration:
-
Intraarticular use
-
Intramuscular use
Product details
Active substance and strength:
-
Prednisolone sodium phosphate33.75/milligram(s)1.00millilitre(s)
Pharmaceutical form:
-
Solution for injection
Anatomical therapeutic chemical veterinary (ATCvet) codes:
- QH02AB06
Legal status of supply:
-
Veterinary medicinal product subject to veterinary prescription
Authorisation status:
-
Valid
Authorised in:
-
Spain
Additional information
Entitlement type:
-
Marketing Authorisation
Legal basis of product authorisation:
-
Full application - Known active substance (Article 12(3) of Directive No 2001/82/EC)
Marketing authorisation holder:
- Fatro Iberica S.L.
Marketing authorisation date:
Manufacturing sites for batch release:
- Fatro S.p.A.
Responsible authority:
- Spanish Agency Of Medicines And Medical Devices
Authorisation number:
- 475 ESP
Date of authorisation status change:
To consult adverse reactions on veterinary medicinal products please go to www.adrreports.eu/vet
Documents
Labelling
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 21/11/2025
Package Leaflet
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 21/11/2025
Summary of Product Characteristics
This document does not exist in this language (English). You can find it in another language below.
Spanish (PDF)
Published on: 21/11/2025
