AKEEGA cpr pell 50mg/500mg 56 pce

7680689770017 Pharmacode 1050908 CH-68977 L01XK52 07.16.4.
AKEEGA cpr pell 50mg/500mg 56 pce
AKEEGA cpr pell 50mg/500mg 56 pce
AKEEGA cpr pell 50mg/500mg 56 pce
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Details

GTIN
7680689770017
Pharmacode
1050908
Product number
6897701
CPT
-
Packaging group
56
Unit
Tablette(n)
Composition
niraparibum 50 mg ut niraparibi tosilas monohydricus 79.7 mg, abirateroni acetas 500 mg corresp. abirateronum 446 mg, hypromellosum, natrii laurilsulfas, lactosum 240.54 mg ut lactosum monohydricum, crospovidonum, cellulosum microcristallinum silicificatum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), E 171, glyceroli monocaprylocapras, talcum, natrii laurilsulfas, E 172 (flavum), E 172 (rubrum), E 172 (nigrum), pro compresso obducto corresp. natrium 5.05 mg.

Articles (1)

Akeega 50 mg/500 mg, Filmtabletten
Filmtabletten
56
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Patient information leaflet
Allemand
22/07/2026
Patient information leaflet
Français
22/07/2026
Patient information leaflet
Italien
22/07/2026
Professional SmPC
Allemand
10/07/2026
Professional SmPC
Français
10/07/2026
Professional SmPC
Italien
10/07/2026

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
Dispensation category
A
First authorization
18/04/2024
Authorization expiration date
17/04/2029
IT number
07.16.4.
Domain
Human medicine
Field of application
Prostatakarzinom

Packaging 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 packaging sizes

AKEEGA cpr pell 100mg/500mg 56 pce
56 TABL
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