Feiba NF 1000 E. (50 E/ml)
Feiba NF 1000 E. (50 E/ml) is a medicine authorised by Swissmedic under authorisation number 41352. The authorisation holder is Takeda Pharma AG. The medicinal product code is Blood products 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 09 August 1979 and the authorisation is valid without a time limit. ATC code B02BD03 places the medicine in the group Antihemorrhagics.
| Authorisation number | 41352 |
|---|---|
| Name | Feiba NF 1000 E. (50 E/ml) |
| Full name | Feiba NF 1000 E. (50 E/ml), Pulver und Lösungsmittel zur Herstellung einer Injektionslösung |
| Authorisation holder | Takeda Pharma AG |
| Medicinal product code | Blood products |
| Dispensing category | B · Prescription only |
| ATC code | B02BD03 |
| First authorisation | 09 August 1979 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 4 | Feiba NF 1000 E. (50 E/ml), Pulver und Lösungsmittel zur Herstellung einer Injektionslösung | B | 15 August 2007 |
| 5 | Feiba NF 2500 E. (50 E/ml), Pulver und Lösungsmittel zur Herstellung einer Injektionslösung | B | 30 September 2010 |
| 6 | Feiba NF 1000 E. (100 E/ml), Pulver und Lösungsmittel zur Herstellung einer Injektionslösung | B | 06 August 2026 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 35 | 1 Durchstechflasche mit Pulver und 1 Durchstechflasche mit Lösungsmittel und Gerätesatz | B02BD03 | 06.01.1. | B | |
| 36 | 1 Durchstechflasche mit Pulver und 1 Durchstechflasche mit Lösungsmittel und Gerätesatz | B02BD03 | 06.01.1. | B | |
| 1 | 1 Durchstechflasche mit Pulver und 1 Durchstechflasche mit Lösungsmittel und Gerätesatz | B02BD03 | 06.01.1. | B |
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Other medicines from this authorisation holder
Frequently asked questions
Is Feiba NF 1000 E. (50 E/ml) authorised in Switzerland?
Yes. Feiba NF 1000 E. (50 E/ml) is authorised by Swissmedic under authorisation number 41352, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Feiba NF 1000 E. (50 E/ml) have?
Feiba NF 1000 E. (50 E/ml) 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 Feiba NF 1000 E. (50 E/ml)?
The authorisation holder is Takeda 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.