Cefuroxim Sandoz 750 mg i.v.
Cefuroxim Sandoz 750 mg i.v. is a medicine authorised by Swissmedic under authorisation number 55823. The authorisation holder is Sandoz Pharmaceuticals AG. The medicinal product code is Synthetic medicines and the dispensing category is A: Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly. First authorisation was granted on 05 February 2003 and the authorisation is valid without a time limit. The export lists no ATC code for this medicine.
| Authorisation number | 55823 |
|---|---|
| Name | Cefuroxim Sandoz 750 mg i.v. |
| Full name | Cefuroxim Sandoz 750 mg i.v., Pulver zur Herstellung einer Injektions-/Infusionslösung |
| Authorisation holder | Sandoz Pharmaceuticals AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | A · Prescription, not repeatable |
| ATC code | not stated |
| First authorisation | 05 February 2003 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 1 | Cefuroxim Sandoz 750 mg i.v., Pulver zur Herstellung einer Injektions-/Infusionslösung | A | 05 February 2003 |
| 2 | Cefuroxim Sandoz 1.5 g i.v., Pulver zur Herstellung einer Injektions-/Infusionslösung | A | 05 February 2003 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| The Swissmedic export lists no pack sizes for this medicine. | |||||
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Other medicines from this authorisation holder
Frequently asked questions
Is Cefuroxim Sandoz 750 mg i.v. authorised in Switzerland?
Yes. Cefuroxim Sandoz 750 mg i.v. is authorised by Swissmedic under authorisation number 55823, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Cefuroxim Sandoz 750 mg i.v. have?
Cefuroxim Sandoz 750 mg i.v. is in dispensing category A. Supplied only against a medical or veterinary prescription that may not be dispensed repeatedly.
Who is the authorisation holder of Cefuroxim Sandoz 750 mg i.v.?
The authorisation holder is Sandoz Pharmaceuticals AG. The holder carries the legal responsibility for quality, safety and product information of the medicine in Switzerland.
Sources
Swissmedic data as of 01 September 2026. No medical advice. Independent directory, not affiliated with Swissmedic or the FOPH.