PROTHROMPLEX NF 600 UI c solv flac 20 ml
7680413300589
CH-41330
B02BD01
06.01.1.
1 / 3
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Details
- Product number
- 4133002
- CPT
- -
- Packaging group
- -
- Unit
- 1 Durchstechflasche Pulver und 1 Durchstechflasche Lösungsmittel mit 1 Gerätesatz
- Composition
- Praeparatio cryodesiccata: proteina plasmatis humani 300-750 mg corresp. factor II coagulationis humanus 600 U.I. et factor VII coagulationis humanus 500 U.I. et factor IX coagulationis humanus 600 U.I. et factor X coagulationis humanus 600 U.I. et proteinum humanum C min. 400 U.I., natrii citras dihydricus, natrii chloridum, heparinum max. 300 U.I., antithrombinum III humanum, pro vitro corresp. natrium 81.7 mg. Solvens: aqua ad iniectabile, pro vitro.
Articles (1)
Prothromplex NF 600 I.E., Pulver und Lösungsmittel zur Herstellung einer Injektionslösung
Pulver
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
aqua ad iniectabile
|
- | Substance | HNIDK |
|
proteina plasmatis humani
|
- | Substance | WIZUS |
|
factor II coagulationis humanus
|
600.0 UI | Substance | Wirkstoff (Principe actif) |
|
factor VII coagulationis humanus
|
500.0 UI | Substance | Wirkstoff (Principe actif) |
|
factor IX coagulationis humanus
|
600.0 UI | Substance | Wirkstoff (Principe actif) |
|
factor X coagulationis humanus
|
600.0 UI | Substance | Wirkstoff (Principe actif) |
|
proteinum humanum C
|
- | Substance | Wirkstoff (Principe actif) |
|
natrii citras dihydricus
|
- | Substance | HNIDK |
|
natrii chloridum
|
- | Substance | HNIDK |
|
heparinum
|
- | Substance | HBESI |
|
antithrombinum III humanum
|
- | Substance | HNIDK |
|
natrium
|
81.7 MG | Substance | HBESI |
Authorization holder
Takeda Pharma AG
8152 Opfikon
Authorization information
- Swissmedic authorization number
- 41330
- Drug name
- Prothromplex NF, Pulver und Lösungsmittel zur Herstellung einer Injektionslösung
- Galenic form
- PULMJ
- ATC Code
- B02BD01
- Authorization status
- Z
- Dispensation category
- B
- First authorization
- 07/08/1979
- Authorization expiration date
- 31/12/9999
- IT number
- 06.01.1.
- Domain
- Human medicine
Packaging details
- Description (FR)
- PROTHROMPLEX NF 600 UI c solv flac 20 ml
- Description (DE)
- PROTHROMPLEX NF 600 IE c Solv Durchstf 20 ml
- Market launch
- 01/09/1993
- Narcotic (BTM)
- No
Application methods
IV