HOLGYEME drag 3 x 21 pce

7680575620044 CH-57562 G03HB01 07.09.0.
HOLGYEME drag 3 x 21 pce
HOLGYEME drag 3 x 21 pce
HOLGYEME drag 3 x 21 pce
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Details

Product number
5756201
CPT
-
Packaging group
3 x 21
Unit
Dragée(s)
Composition
cyproteroni acetas 2 mg, ethinylestradiolum 35 µg, lactosum monohydricum 29.115 mg, maydis amylum, povidonum K 25, talcum, magnesii stearas, saccharum 19.637 mg, calcii carbonas, povidonum K 90, macrogolum 6000, glycerolum (85 per centum), cera montanglycoli, E 171, E 172, pro compresso obducto.

Articles (1)

Holgyeme, comprimé pelliculé
comprimé pelliculé
3 x 21
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Patient information leaflet
Allemand
11/02/2022
Patient information leaflet
Français
11/02/2022
Patient information leaflet
Italien
11/02/2022
Professional SmPC
Allemand
11/02/2022
Professional SmPC
Français
11/02/2022

Detailed composition

Substance Quantity Type Category
(N/A)
2.0 MG Substance Wirkstoff (Principe actif)
(N/A)
35.0 UG Substance Wirkstoff (Principe actif)
(N/A)
29.115 MG Substance HBESI
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
- Substance HNIDK
(N/A)
19.637 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 HNIDK
(N/A)
- Substance FTODK

Authorization holder

EFFIK SA

1260 Nyon

Authorization information

Swissmedic authorization number
57562
Drug name
Holgyeme, comprimé pelliculé
Galenic form
FILM
ATC Code
G03HB01
Authorization status
Z
Dispensation category
B
First authorization
13/12/2006
Authorization expiration date
31/12/9999
IT number
07.09.0.
Domain
Human medicine

Packaging details

Description (FR)
HOLGYEME drag 3 x 21 pce
Description (DE)
HOLGYEME Drag 3 x 21 Stk
Market launch
13/12/2006
Narcotic (BTM)
No

Other packaging sizes

HOLGYEME drag 21 pce
1 x 21 DRG
View