TRIKAFTA cpr pell 50mg/25mg/37.5mg + 75mg 84 pce

7680677730023 CH-67773 R07AX32 03.99.0.

Reimbursement limitations:

TRIKAFTA_150

Après garantie de prise en charge des frais par l’assureur et après consultation préalable du …

TRIKAFTA cpr pell 50mg/25mg/37.5mg + 75mg 84 pce
TRIKAFTA cpr pell 50mg/25mg/37.5mg + 75mg 84 pce
TRIKAFTA cpr pell 50mg/25mg/37.5mg + 75mg 84 pce
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Details

Product number
6777302
CPT
-
Packaging group
84 (4 x 21)
Unit
Tablette(n)
Composition
Filmtablette Morgendosis (elexacaftorum 50 mg / tezacaftorum 25 mg / ivacaftorum 37.5 mg): elexacaftorum 50 mg, tezacaftorum 25 mg, ivacaftorum 37.5 mg, hypromellosum, hypromellosi acetas succinas, natrii laurilsulfas, carmellosum natricum conexum, cellulosum microcristallinum, magnesii stearas, Überzug: hypromellosum, hydroxypropylcellulosum, E 171, talcum, E 172 (flavum), E 172 (rubrum) pro compresso obducto corresp. natrium 1.34 mg. Filmtablette Abenddosis (ivacaftorum 75 mg): ivacaftorum 75 mg, hypromellosi acetas succinas, natrii laurilsulfas, cellulosum microcristallinum, lactosum monohydricum 83.6 mg, carmellosum natricum conexum, silica colloidalis anhydrica, magnesii stearas, Überzug: poly(alcohol vinylicus), E 171, macrogolum 3350, talcum, E 132, cera carnauba, Drucktinte: lacca, E 172 (nigrum), propylenglycolum, ammonii hydroxidum pro compresso obducto corresp. natrium 0.9 mg.

Articles (1)

Trikafta 50 mg / 25 mg / 37.5 mg, 75 mg, Filmtabletten
Filmtabletten
84 (4 x 21)
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Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Professional SmPC
Allemand
01/10/2025
Professional SmPC
Français
01/10/2025
Professional SmPC
Italien
01/10/2025
Patient information leaflet
Allemand
27/06/2025
Patient information leaflet
Français
27/06/2025
Patient information leaflet
Italien
27/06/2025

Detailed composition

Substance Quantity Type Category
FTAB
50.0 MG Substance Wirkstoff (Principe actif)
FTAB
75.0 MG Substance Wirkstoff (Principe actif)
FTAB
25.0 MG Substance Wirkstoff (Principe actif)
FTAB
- Substance HNIDK
FTAB
- Substance Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration)
FTAB
37.5 MG Substance Wirkstoff (Principe actif)
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
83.6 MG Substance HBESI
FTAB
- Substance Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration)
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance FNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance FNIDK
FTAB
- Substance HNIDK
FTAB
- Substance HNIDK
FTAB
- Substance FIMDK
FTAB
- Substance FTODK
FTAB
- Substance HNIDK
FTAB
- Substance FTODK
FTAB
- Substance HNIDK
FTAB
- Substance FTODK
FTAB
1.34 MG Substance HBESI
FTAB
- Substance Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration)
FTAB
- Substance HNIDK
FTAB
0.9 MG Substance HBESI

Reimbursement information

Public price
CHF 14565.30
Specialties list
Yes
Generic
No

Reimbursement limitation

SL addition date: 01/05/2022

Authorization holder

Vertex Pharmaceuticals (CH) GmbH

6300 Zug

Authorization information

Swissmedic authorization number
67773
Drug name
Trikafta, Filmtabletten
Galenic form
TAB
ATC Code
R07AX32
Authorization status
Z
Dispensation category
A
First authorization
10/12/2020
Authorization expiration date
31/12/9999
IT number
03.99.0.
Domain
Human medicine
Field of application
Mukoviszidose

Packaging details

Description (FR)
TRIKAFTA cpr pell 50mg/25mg/37.5mg + 75mg 84 pce
Description (DE)
TRIKAFTA Filmtabl 50mg/25mg/37.5mg + 75mg 84 Stk
Market launch
05/01/2022
Narcotic (BTM)
No

Other packaging sizes

TRIKAFTA cpr pell 100mg/50mg/75mg + 150mg 84 pce
84 (4 x 21) TABL
View