BUSCOPAN drag 10 mg 40 pce

7680173530158 CH-17353 A03BB01 04.02.0.
BUSCOPAN drag 10 mg 40 pce
BUSCOPAN drag 10 mg 40 pce
BUSCOPAN drag 10 mg 40 pce
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Details

Product number
1735301
CPT
-
Packaging group
40
Unit
Dragée(s)
Composition
scopolamini butylbromidum 10 mg, calcii hydrogenophosphas, maydis amylum, amylum solubile, silica colloidalis anhydrica, acidum tartaricum, acidum stearicum, Überzug: povidonum K 25, saccharum 41.182 mg, talcum, acaciae gummi, macrogolum 6000, cera carnauba, cera alba, E 171, pro compresso obducto.

Articles (1)

Buscopan, Dragées
Dragées
40
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Patient information leaflet
Allemand
27/05/2024
Patient information leaflet
Français
27/05/2024
Patient information leaflet
Italien
27/05/2024
Professional SmPC
Allemand
27/05/2024
Professional SmPC
Français
27/05/2024
Professional SmPC
Italien
27/05/2024

Detailed composition

Substance Quantity Type Category
(N/A)
10.0 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)
41.182 MG Substance HBESI
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance FNIDK

Authorization holder

Opella Healthcare Switzerland AG

6343 Risch

Authorization information

Swissmedic authorization number
17353
Drug name
Buscopan, Dragées
Galenic form
UEBT
ATC Code
A03BB01
Authorization status
Z
Dispensation category
D
First authorization
14/06/1952
Authorization expiration date
31/12/9999
IT number
04.02.0.
Domain
Human medicine
Field of application
Spasmolyticum

Packaging details

Description (FR)
BUSCOPAN drag 10 mg 40 pce
Description (DE)
BUSCOPAN Drag 10 mg 40 Stk
Market launch
14/06/1952
Narcotic (BTM)
No

Other packaging sizes

BUSCOPAN drag 10 mg 50 pce
50 DRG
View
BUSCOPAN drag 10 mg 20 pce
20 DRG
View