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Details
- Product number
- 5385701
- CPT
- -
- Packaging group
- 5
- Unit
- Durchstechflasche(n)
- Composition
- Praeparatio sicca: topotecanum 4 mg ut topotecani hydrochloridum, acidum tartaricum, mannitolum, acidum hydrochloridum aut natrii hydroxidum, pro vitro corresp. natrium 1.68 mg.
Articles (1)
Hycamtin 4 mg, Lyophilisat
Lyophilisat
5
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
topotecanum
|
4.0 MG | Substance | Wirkstoff (Principe actif) |
|
topotecani hydrochloridum
|
- | Substance | WIZUS |
|
acidum tartaricum
|
- | Substance | HNIDK |
|
mannitolum
|
- | Substance | HNIDK |
|
acidum hydrochloridum
|
- | Substance | HNIDK |
|
natrii hydroxidum
|
- | Substance | HNIDK |
|
natrium
|
1.68 MG | Substance | HBESI |
Authorization holder
Sandoz Pharmaceuticals AG
6343 Risch
Authorization information
- Swissmedic authorization number
- 53857
- Drug name
- Hycamtin, Lyophilisat
- Galenic form
- PULPA
- ATC Code
- L01XX17
- Authorization status
- Z
- Dispensation category
- A
- First authorization
- 16/10/1996
- Authorization expiration date
- 31/12/9999
- IT number
- 07.16.1.
- Domain
- Human medicine
Packaging details
- Description (FR)
- HYCAMTIN subst sèche 4 mg flac 5 pce
- Description (DE)
- HYCAMTIN Trockensub 4 mg Durchstf 5 Stk
- Market launch
- 16/10/1996
- Market withdrawal
- 06/03/2026
- Narcotic (BTM)
- No