Ibu Sandoz Plus 200 mg / 500 mg, Filmtabletten

7680686700024 CH-68670 Filmtabletten

Associated product:

IBU Sandoz Plus cpr pell 200 mg/500 mg 20 pce
Ibu Sandoz Plus 200 mg / 500 mg, Filmtabletten
Ibu Sandoz Plus 200 mg / 500 mg, Filmtabletten
Ibu Sandoz Plus 200 mg / 500 mg, Filmtabletten
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Article details

Package size
20
Selling units
20
Measure
Tablette(n)
Galenic form
Filmtabletten
Galenic group
Tabletten

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Patient information leaflet
Allemand
07/05/2025
Patient information leaflet
Français
07/05/2025
Patient information leaflet
Italien
07/05/2025
Summary of Product Characteristics
Allemand
07/05/2025
Summary of Product Characteristics
Français
07/05/2025
Summary of Product Characteristics
Italien
07/05/2025

Detailed composition

Substance Quantity Type Category
(N/A)
200.0 MG Substance Wirkstoff (Principe actif)
(N/A)
500.0 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)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance FNIDK

Authorization holder

Sandoz Pharmaceuticals AG

6343 Risch

Authorization information

Swissmedic authorization number
68670
Drug name
Ibu Sandoz Plus, Filmtabletten
Galenic form
FILM
ATC Code
N02BE51
Authorization status
Z
Dispensing category
D
First authorization
07/07/2022
Authorization expiration date
06/07/2027
IT Number
01.01.2.
Domain
Human medicine
Field of application
Zur kurzzeitigen symptomatischen Behandlung von leichten bis mässig starken Schmerzen.

Package details

Description (FR)
IBU Sandoz Plus cpr pell 200 mg/500 mg 20 pce
Description (DE)
IBU Sandoz Plus Filmtabl 200 mg/500 mg 20 Stk
Market launch
07/07/2022
Market withdrawal
01/10/2025
Narcotic (BTM)
No

Other package sizes (1)

None
10 TABL
GTIN: None
Not in V1