|
Prednisolonacetat-Injektionssuspension
|
10 mg/ml
|
V/NRP/95/0123
|
AS Dimedium Latvija, Latvija
|
QH02AB06
|
cattle; horses; dogs; cats
|
|
Medicinal product information
| Pharmaceutical form: |
suspension for injection
|
| International name (active substance): |
Prednisolone acetate
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Produlab Pharma b.v., Nīderlande
|
| Date of authorisation/renewal: |
21-May-2008
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
NRP
|
| Package leaflet: |
[DOCX] 18122020LI (18-Dec-2020)
|
| Labelling text: |
[DOCX] 18122020M (18-Dec-2020)
|
| Summary of product characteristics: |
[DOCX] 18122020ZA (18-Dec-2020)
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| V/NRP/95/0123-01 |
10 mg/ml |
1 |
Flakons, 100 ml |
-
|
| V/NRP/95/0123-02 |
10 mg/ml |
12 |
Flakons, 100 ml |
-
|
|