Akeega 50 mg/500 mg, Filmtabletten
7680689770017
CH-68977
Filmtabletten
Associated product:
AKEEGA cpr pell 50mg/500mg 56 pce
1 / 3
google
Article details
- Package size
- 56
- Selling units
- 56
- Measure
- Tablette(n)
- Galenic form
- Filmtabletten
- Galenic group
- Tabletten
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
niraparibum
|
50.0 MG | Substance | Wirkstoff (Principe actif) |
|
niraparibi tosilas monohydricus
|
79.7 MG | Substance | WIZUS |
|
abirateroni acetas
|
500.0 MG | Substance | Wirkstoff (Principe actif) |
|
abirateronum
|
446.0 MG | Substance | WIIS |
|
hypromellosum
|
- | Substance | HNIDK |
|
natrii laurilsulfas
|
- | Substance | Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration) |
|
lactosum
|
240.54 MG | Substance | HBESI |
|
lactosum monohydricum
|
- | Substance | HNIDK |
|
crospovidonum
|
- | Substance | HNIDK |
|
cellulosum microcristallinum silicificatum
|
- | Substance | HNIDK |
|
silica colloidalis anhydrica
|
- | Substance | HNIDK |
|
magnesii stearas
|
- | Substance | HNIDK |
|
poly(alcohol vinylicus)
|
- | Substance | HNIDK |
|
E 171
|
- | Substance | FNIDK |
|
glyceroli monocaprylocapras
|
- | Substance | HNIDK |
|
talcum
|
- | Substance | HNIDK |
|
natrii laurilsulfas
|
- | Substance | Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration) |
|
E 172 (flavum)
|
- | Substance | FTODK |
|
E 172 (rubrum)
|
- | Substance | FTODK |
|
E 172 (nigrum)
|
- | Substance | FTODK |
|
natrium
|
5.05 MG | Substance | HBESI |
Reimbursement information
Public price
CHF 4523.30
Specialties list
Yes
Generic
No
Reimbursement limitation
SL addition date:
01/07/2024
Authorization holder
Janssen-Cilag AG
6300 Zug
Authorization information
- Swissmedic authorization number
- 68977
- Drug name
- Akeega, Filmtabletten
- Galenic form
- FILM
- ATC Code
- L01XK52
- Authorization status
- Z
- Dispensing category
- A
- First authorization
- 18/04/2024
- Authorization expiration date
- 17/04/2029
- IT Number
- 07.16.4.
- Domain
- Human medicine
Package details
- Description (FR)
- AKEEGA cpr pell 50mg/500mg 56 pce
- Description (DE)
- AKEEGA Filmtabl 50mg/500mg 56 Stk
- Market launch
- 27/05/2024
- Narcotic (BTM)
- No
Other package sizes (1)
AKEEGA cpr pell 100mg/500mg 56 pce
56 TABL
GTIN: 7680689770024