Actemra 400 mg/20 ml, Konzentrat zur Herstellung einer Infusionslösung

7680588680035 CH-58868 Konzentrat
Actemra 400 mg/20 ml, Konzentrat zur Herstellung einer Infusionslösung
Actemra 400 mg/20 ml, Konzentrat zur Herstellung einer Infusionslösung
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Article details

Package size
1
Selling units
1
Measure
Durchstechflasche(n)
Galenic form
Konzentrat
Galenic group
Tinkturen/Desinfektion

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Summary of Product Characteristics
Allemand
03/08/2023
Summary of Product Characteristics
Français
03/08/2023
Summary of Product Characteristics
Italien
03/08/2023

Detailed composition

Substance Quantity Type Category
(N/A)
400.0 MG Substance Wirkstoff (Principe actif)
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
8.84 MG Substance HBESI

Reimbursement information

Public price
CHF 722.00
Specialties list
Yes
Generic
No

Reimbursement limitation

SL addition date: 01/05/2009

Authorization holder

Roche Pharma (Schweiz) AG

4058 Basel

Authorization information

Swissmedic authorization number
58868
Drug name
Actemra, Konzentrat zur Herstellung einer Infusionslösung
Galenic form
LSPA
ATC Code
L04AC07
Authorization status
Z
Dispensing category
A
First authorization
02/12/2008
Authorization expiration date
31/12/9999
IT Number
07.15.0.
Domain
Human medicine
Field of application
Rheumatoide Arthritis. Systemische juvenile idiopathische Arthritis. Polyartikuläre juvenile idiopathische Arthritis. Zytokinfreisetzungssyndrom.

Package details

Description (FR)
ACTEMRA conc perf 400 mg/20 ml flac 20 ml
Description (DE)
ACTEMRA Inf Konz 400 mg/20 ml Durchstf 20 ml
Market launch
02/12/2008
Narcotic (BTM)
No

Other package sizes (2)

ACTEMRA conc perf 80 mg/4 ml flac 4 ml
1 DUR
GTIN: 7680588680011
View
ACTEMRA conc perf 200 mg/10 ml flac 10 ml
1 DUR
GTIN: 7680588680028
View