|
Naxcel
|
100 mg/ml
|
EU/2/05/053/001
|
Zoetis Belgium S.A., Beļģija
|
QJ01DD90
|
pigs
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
suspension for injection
|
| International name (active substance): |
Ceftiofur
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Zoetis Belgium S.A., Beļģija
|
| Date of authorisation/renewal: |
26-May-2010
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
EU
|
| Package leaflet: |
*
-
|
| Labelling text: |
*
-
|
| Summary of product characteristics: |
*
-
|
|
*
More detailed information available on the European Medicines Agency website
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| EU/2/05/053/001 |
100 mg/ml |
1 |
Stikla flakons, 100 ml |
-
|
|
|
Naxcel
|
100 mg/ml
|
EU/2/05/053/002
|
Zoetis Belgium S.A., Beļģija
|
QJ01DD90
|
pigs
|
|
Medicinal product information
| Pharmaceutical form: |
suspension for injection
|
| International name (active substance): |
Ceftiofur
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Zoetis Belgium S.A., Beļģija
|
| Date of authorisation/renewal: |
26-May-2010
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
EU
|
| Package leaflet: |
*
-
|
| Labelling text: |
*
-
|
| Summary of product characteristics: |
*
-
|
|
*
More detailed information available on the European Medicines Agency website
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| EU/2/05/053/002 |
100 mg/ml |
1 |
Stikla flakons, 50 ml |
-
|
|
|
Naxcel
|
200 mg/ml
|
EU/2/05/053/003
|
Zoetis Belgium S.A., Beļģija
|
QJ01DD90
|
cattle
|
Vairāk
|
Medicinal product information
| Pharmaceutical form: |
suspension for injection
|
| International name (active substance): |
Ceftiofur
|
| Distribution category: |
To be supplied only on veterinary prescription
|
| Manufacturer(s) responsible for batch release |
Zoetis Belgium S.A., Beļģija
|
| Date of authorisation/renewal: |
26-May-2010
|
| Marketing authorisation valid until: |
Unlimited time period
|
| Marketing authorisation procedure: |
EU
|
| Package leaflet: |
*
-
|
| Labelling text: |
*
-
|
| Summary of product characteristics: |
*
-
|
|
*
More detailed information available on the European Medicines Agency website
|
Products
| ID |
Strength |
Package size |
Primary packaging |
Labelling |
| EU/2/05/053/003 |
200 mg/ml |
1 |
Stikla flakons, 100 ml |
-
|
|