OCREVUS sous-cutané sol inj 920 mg/23 ml flac

7680689880013 CH-68988 L04AG08 01.99.0.

Reimbursement limitations:

OCREVUS.01

Pour le traitement des patients adultes atteints de formes actives de sclérose en plaques (SEP) …

OCREVUS sous-cutané sol inj 920 mg/23 ml flac
OCREVUS sous-cutané sol inj 920 mg/23 ml flac
OCREVUS sous-cutané sol inj 920 mg/23 ml flac
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Details

Product number
6898801
CPT
-
Packaging group
1
Unit
Durchstechflasche(n)
Composition
ocrelizumabum 920 mg, hyaluronidasum humanum ADNr, trehalosum dihydricum, acidum aceticum glaciale, methioninum, polysorbatum 20, natrii acetas trihydricus, aqua ad iniectabile ad solutionem pro 23 ml corresp. natrium 8.4 mg.

Articles (1)

Ocrevus subkutan 920 mg/23 ml, Injektionslösung
Injektionslösung
1
View

Official Swissmedic V2 data

Additional information from the official database

Detailed composition

Substance Quantity Type Category
(N/A)
920.0 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)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
8.4 MG Substance HBESI

Reimbursement information

Public price
CHF 9813.60
Specialties list
Yes
Generic
No

Reimbursement limitation

SL addition date: 01/02/2025

Authorization holder

Roche Pharma (Schweiz) AG

4058 Basel

Authorization information

Swissmedic authorization number
68988
Drug name
Ocrevus subkutan, Injektionslösung
Galenic form
LSINJ
ATC Code
L04AG08
Authorization status
Z
Dispensation category
A
First authorization
15/11/2024
Authorization expiration date
14/11/2029
IT number
01.99.0.
Domain
Human medicine
Field of application
Multiple Sklerose

Packaging details

Description (FR)
OCREVUS sous-cutané sol inj 920 mg/23 ml flac
Description (DE)
OCREVUS subkutan Inj Lös 920 mg/23 ml Durchstf
Market launch
15/11/2024
Narcotic (BTM)
No