Vydura 75 mg, Lyophilisat zum Einnehmen

7680690350031 CH-69035 Lyophilisat
Vydura 75 mg, Lyophilisat zum Einnehmen
Vydura 75 mg, Lyophilisat zum Einnehmen
Vydura 75 mg, Lyophilisat zum Einnehmen
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Article details

Package size
16
Selling units
16
Measure
Einzeldose(n)
Galenic form
Lyophilisat
Galenic group
Lösbar zur Injektion/Infusion

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Summary of Product Characteristics
Allemand
16/07/2026
Summary of Product Characteristics
Français
16/07/2026
Summary of Product Characteristics
Italien
16/07/2026
Patient information leaflet
Allemand
15/07/2026
Patient information leaflet
Français
15/07/2026
Patient information leaflet
Italien
15/07/2026

Detailed composition

Substance Quantity Type Category
rimegepantum
75.0 MG Substance Wirkstoff (Principe actif)
rimegepanti hemisulfas sesquihydricus
- Substance WIZUS
gelatina
- Substance HNIDK
mannitolum
- Substance HNIDK
sucralosum
- Substance HNIDK
aromatica
- Substance AROMA
alcohol benzylicus
- Substance HBESI

Reimbursement information

Public price
CHF 377.30
Specialties list
Yes
Generic
No

Reimbursement limitation

SL addition date: 01/05/2024

Authorization holder

Pfizer AG

8052 Zürich

Authorization information

Swissmedic authorization number
69035
Drug name
Vydura, Lyophilisat zum Einnehmen
Galenic form
LYO
ATC Code
N02CD06
Authorization status
Z
Dispensing category
B
First authorization
18/10/2023
Authorization expiration date
17/10/2028
IT Number
02.05.1.
Domain
Human medicine
Field of application
Migränemittel

Package details

Description (FR)
VYDURA ODT cpr orodisp 75 mg 16 pce
Description (DE)
VYDURA ODT Schmelztabl 75 mg 16 Stk
Market launch
18/10/2023
Narcotic (BTM)
No

Other package sizes (2)

VYDURA ODT cpr orodisp 75 mg 2 pce
2 EINZ
GTIN: 7680690350017
View
VYDURA ODT cpr orodisp 75 mg 8 pce
8 EINZ
GTIN: 7680690350024
View
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