TEICOPLANIN Evultis subst sèche 400 mg c solv
7680588080064
CH-58808
J01XA02
08.01.9.
1 / 2
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Details
- Product number
- 5880802
- CPT
- -
- Packaging group
- 1 + 1
- Unit
- Durchstechflasche(n)
- Composition
- Praeparatio cryodesiccata: teicoplaninum 400 mg, natrii chloridum, natrii hydroxidum ad pH, pro vitro corresp. natrium 10 mg. Solvens: aqua ad iniectabile 3 ml.
Articles (1)
Teicoplanin-Evultis 400 mg, Polvere e solvente per soluzione iniettabile / per infusione / soluzione orale
soluzione
1 + 1
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
PRC
|
400.0 MG | Substance | Wirkstoff (Principe actif) |
|
SOLV
|
3.0 ML | Substance | HNIDK |
|
PRC
|
- | Substance | HNIDK |
|
PRC
|
- | Substance | HNIDK |
|
PRC
|
10.0 MG | Substance | HBESI |
Authorization holder
Evultis SA
6855 Stabio
Authorization information
- Swissmedic authorization number
- 58808
- Drug name
- Teicoplanin-Evultis, Polvere e solvente per soluzione iniettabile / per infusione / soluzione orale
- Galenic form
- PULP
- ATC Code
- J01XA02
- Authorization status
- Z
- Dispensation category
- A
- First authorization
- 03/04/2009
- Authorization expiration date
- 31/12/9999
- IT number
- 08.01.9.
- Domain
- Human medicine
Packaging details
- Description (FR)
- TEICOPLANIN Evultis subst sèche 400 mg c solv
- Description (DE)
- TEICOPLANIN Evultis Trockensub 400 mg c Solv
- Market launch
- 03/04/2009
- Narcotic (BTM)
- No