PRETUFEN rhume&douleurs liés refroidiss 20 pce

7680676740030 CH-67674 M01AE51 07.10.2.

Active substances:

PRETUFEN rhume&douleurs liés refroidiss 20 pce
PRETUFEN rhume&douleurs liés refroidiss 20 pce
PRETUFEN rhume&douleurs liés refroidiss 20 pce
PRETUFEN rhume&douleurs liés refroidiss 20 pce
1 / 4
Fiches Amavita / Sun Store / Coop Vitality

Details

Product number
6767401
CPT
-
Packaging group
20
Unit
Tablette(n)
Composition
ibuprofenum 200 mg, pseudoephedrini hydrochloridum 30 mg, silica colloidalis anhydrica, carmellosum natricum conexum, cellulosum microcristallinum, calcii hydrogenophosphas dihydricus, magnesii stearas, maydis amylum, Überzug: hypromellosum, macrogolum 400, talcum, E 171, E 172 (flavum), pro compresso obducto corresp. natrium 450 µg.

Articles (1)

Pretufen Schnupfen und Erkältungsschmerzen 200 mg/30 mg, Filmtabletten
Filmtabletten
20
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Professional SmPC
Allemand
17/03/2025
Professional SmPC
Français
17/03/2025
Professional SmPC
Italien
17/03/2025
Patient information leaflet
Allemand
01/03/2025
Patient information leaflet
Français
01/03/2025
Patient information leaflet
Italien
01/03/2025

Detailed composition

Substance Quantity Type Category
ibuprofenum
200.0 MG Substance Wirkstoff (Principe actif)
pseudoephedrini hydrochloridum
30.0 MG Substance Wirkstoff (Principe actif)
silica colloidalis anhydrica
- Substance HNIDK
carmellosum natricum conexum
- Substance HNIDK
cellulosum microcristallinum
- Substance HNIDK
calcii hydrogenophosphas dihydricus
- Substance HNIDK
magnesii stearas
- Substance HNIDK
maydis amylum
- Substance HNIDK
hypromellosum
- Substance HNIDK
macrogolum 400
- Substance Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration)
talcum
- Substance HNIDK
E 171
- Substance FNIDK
E 172 (flavum)
- Substance FTODK
natrium
450.0 UG Substance HBESI

Authorization holder

Bayer (Schweiz) AG

8045 Zürich

Authorization information

Swissmedic authorization number
67674
Drug name
Pretufen Schnupfen und Erkältungsschmerzen, Filmtabletten
Galenic form
FILM
ATC Code
M01AE51
Authorization status
Z
Dispensation category
D
First authorization
16/04/2021
Authorization expiration date
31/12/9999
IT number
07.10.2.
Domain
Human medicine
Field of application
Zur kurzzeitigen symptomatischen Behandlung bei Erkältungskrankheiten

Packaging details

Description (FR)
PRETUFEN rhume&douleurs liés refroidiss 20 pce
Description (DE)
PRETUFEN Schnupfen&Erkältungsschmerzen 20 Stk
Market launch
16/04/2021
Narcotic (BTM)
No

Other packaging sizes

Buy us a coffee Explore the data