Floxapen 500 mg i.v./i.m.
Floxapen 500 mg i.v./i.m. is a medicine authorised by Swissmedic under authorisation number 37404. The authorisation holder is Teva Pharma AG. The medicinal product code is Synthetic medicines and the dispensing category is B: Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly. First authorisation was granted on 16 November 1972 and the authorisation is valid without a time limit. ATC code J01CF05 places the medicine in the group Antibacterials for systemic use.
| Authorisation number | 37404 |
|---|---|
| Name | Floxapen 500 mg i.v./i.m. |
| Full name | Floxapen 500 mg i.v./i.m., Pulver zur Herstellung einer Injektions-/Infusionslösung |
| Authorisation holder | Teva Pharma AG |
| Medicinal product code | Synthetic medicines |
| Dispensing category | B · Prescription only |
| ATC code | J01CF05 |
| First authorisation | 16 November 1972 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 2 | Floxapen 500 mg i.v./i.m., Pulver zur Herstellung einer Injektions-/Infusionslösung | B | 16 November 1972 |
| 3 | Floxapen 1 g i.v./i.m., Pulver zur Herstellung einer Injektions-/Infusionslösung | B | 16 November 1972 |
| 4 | Floxapen 2 g i.v., Pulver zur Herstellung einer Injektions-/Infusionslösung | B | 11 April 2012 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 20 | 10 | Durchstechflasche(n) | J01CF05 | 08.01.24 | B |
| 39 | 10 | Durchstechflasche(n) | J01CF05 | 08.01.24 | B |
| 40 | 10 | Durchstechflasche(n) | J01CF05 | 08.01.24 | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Floxapen 500 mg i.v./i.m. authorised in Switzerland?
Yes. Floxapen 500 mg i.v./i.m. is authorised by Swissmedic under authorisation number 37404, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Floxapen 500 mg i.v./i.m. have?
Floxapen 500 mg i.v./i.m. is in dispensing category B. Supplied only against a prescription which, at the prescriber's discretion, may be dispensed repeatedly.
Who is the authorisation holder of Floxapen 500 mg i.v./i.m.?
The authorisation holder is Teva Pharma 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.