Prothromplex NF 600 I.E.
Prothromplex NF 600 I.E. is a medicine authorised by Swissmedic under authorisation number 41330. 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 07 August 1979 and the authorisation is valid without a time limit. ATC code B02BD01 places the medicine in the group Antihemorrhagics.
| Authorisation number | 41330 |
|---|---|
| Name | Prothromplex NF 600 I.E. |
| Full name | Prothromplex NF 600 I.E., Pulver und Lösungsmittel zur Herstellung einer Injektionslösung |
| Authorisation holder | Takeda Pharma AG |
| Medicinal product code | Blood products |
| Dispensing category | B · Prescription only |
| ATC code | B02BD01 |
| First authorisation | 07 August 1979 |
| Authorisation validity | unlimited |
| No. | Name | Dispensing category | Authorisation date |
|---|---|---|---|
| 2 | Prothromplex NF 600 I.E., Pulver und Lösungsmittel zur Herstellung einer Injektionslösung | B | 01 September 1993 |
| 3 | Prothromplex NF 500 I.E., Pulver und Lösungsmittel zur Herstellung einer Injektionslösung | B | 16 January 2024 |
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| Pack code | Quantity | Unit | ATC | IT code | Dispensing category |
|---|---|---|---|---|---|
| 58 | 1 Durchstechflasche Pulver und 1 Durchstechflasche Lösungsmittel mit 1 Gerätesatz | B02BD01 | 06.01.1. | B | |
| 1 | 1 Durchstechflasche Pulver und 1 Durchstechflasche Lösungsmittel und 1 Mix2Vial | B02BD01 | 06.01.1. | B |
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Medicines in the same ATC group
Other medicines from this authorisation holder
Frequently asked questions
Is Prothromplex NF 600 I.E. authorised in Switzerland?
Yes. Prothromplex NF 600 I.E. is authorised by Swissmedic under authorisation number 41330, data as of 01 September 2026. The authorisation is valid without a time limit.
Which dispensing category does Prothromplex NF 600 I.E. have?
Prothromplex NF 600 I.E. 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 Prothromplex NF 600 I.E.?
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.