SUMATRIPTAN Zentiva cpr pell 50 mg 12 pce
7680594640047
CH-59464
N02CC01
02.05.1.
Active substances:
1 / 3
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Details
- Product number
- 5946401
- CPT
- -
- Packaging group
- 12
- Unit
- Tablette(n)
- Composition
- sumatriptanum 50 mg ut sumatriptani succinas 70 mg, lactosum monohydricum 70 mg, carmellosum natricum conexum corresp. natrium 0.135 mg, cellulosum microcristallinum, silica colloidalis anhydrica, magnesii stearas, Überzug: hypromellosum, lactosum monohydricum 1.1 mg, macrogolum 3000, triacetinum, E 171, E 172 (rubrum), E 172 (flavum), E 172 (nigrum), pro compresso obducto.
Articles (1)
Sumatriptan Zentiva 50 mg, Filmtabletten
Filmtabletten
12
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
sumatriptanum
|
50.0 MG | Substance | Wirkstoff (Principe actif) |
|
sumatriptani succinas
|
70.0 MG | Substance | WIZUS |
|
lactosum monohydricum
|
70.0 MG | Substance | HBESI |
|
carmellosum natricum conexum
|
- | Substance | HNIDK |
|
natrium
|
0.135 MG | Substance | HBESI |
|
cellulosum microcristallinum
|
- | Substance | HNIDK |
|
silica colloidalis anhydrica
|
- | Substance | HNIDK |
|
magnesii stearas
|
- | Substance | HNIDK |
|
hypromellosum
|
- | Substance | HNIDK |
|
lactosum monohydricum
|
1.1 MG | Substance | HBESI |
|
macrogolum 3000
|
- | Substance | HNIDK |
|
triacetinum
|
- | Substance | HNIDK |
|
E 171
|
- | Substance | FNIDK |
|
E 172 (rubrum)
|
- | Substance | FTODK |
|
E 172 (flavum)
|
- | Substance | FTODK |
|
E 172 (nigrum)
|
- | Substance | FTODK |
Reimbursement information
Public price
CHF 50.60
Specialties list
Yes
Generic
Yes
SL addition date:
01/05/2009
Authorization holder
Helvepharm AG
8500 Frauenfeld
Authorization information
- Swissmedic authorization number
- 59464
- Drug name
- Sumatriptan Zentiva 50 mg, Filmtabletten
- Galenic form
- FILM
- ATC Code
- N02CC01
- Authorization status
- Z
- Authorization category
- Category C
- Dispensation category
- B
- First authorization
- 19/12/2008
- Authorization expiration date
- 31/12/9999
- IT number
- 02.05.1.
- Domain
- Human medicine
Packaging details
- Description (FR)
- SUMATRIPTAN Zentiva cpr pell 50 mg 12 pce
- Description (DE)
- SUMATRIPTAN Zentiva Filmtabl 50 mg 12 Stk
- Market launch
- 19/12/2008
- Narcotic (BTM)
- No