FEMINAC 35 drag 2 mg 21 pce

7680567220016 CH-56722 G03HB01 07.09.0.

Active substances:

FEMINAC 35 drag 2 mg 21 pce
Fiches Amavita / Sun Store / Coop Vitality

Details

Product number
5672201
CPT
-
Packaging group
21
Unit
Dragée(s)
Composition
ethinylestradiolum 0.035 mg, cyproteroni acetas 2 mg, lactosum monohydricum 41.19 mg, cellulosum microcristallinum, povidonum K 30, carmellosum natricum conexum corresp. natrium 0.29 mg, magnesii stearas, Überzug: hypromellosum, macrogolum 400, lacca, cera alba, cera carnauba, saccharum 10.358 mg, E 104, E 132, E 171, E 172 (flavum), E 172 (rubrum), E 172 (nigrum), pro compresso obducto.

Articles (1)

Feminac 35, Dragées
Dragées
21
View

Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Patient information leaflet
Allemand
29/05/2026
Patient information leaflet
Français
29/05/2026
Patient information leaflet
Italien
29/05/2026
Professional SmPC
Allemand
29/05/2026
Professional SmPC
Français
29/05/2026
Professional SmPC
Italien
29/05/2026

Detailed composition

Substance Quantity Type Category
ethinylestradiolum
0.035 MG Substance Wirkstoff (Principe actif)
cyproteroni acetas
2.0 MG Substance Wirkstoff (Principe actif)
lactosum monohydricum
41.19 MG Substance HBESI
cellulosum microcristallinum
- Substance HNIDK
povidonum K 30
- Substance HNIDK
carmellosum natricum conexum
- Substance HNIDK
natrium
0.29 MG Substance HBESI
magnesii stearas
- Substance HNIDK
hypromellosum
- Substance HNIDK
macrogolum 400
- Substance Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration)
lacca
- Substance HNIDK
cera alba
- Substance HNIDK
cera carnauba
- Substance HNIDK
saccharum
10.358 MG Substance HBESI
E 104
- Substance FIMDK
E 132
- Substance FIMDK
E 171
- Substance FNIDK
E 172 (flavum)
- Substance FTODK
E 172 (rubrum)
- Substance FTODK
E 172 (nigrum)
- Substance FTODK

Authorization holder

Spirig HealthCare AG

4622 Egerkingen

Authorization information

Swissmedic authorization number
56722
Drug name
Feminac 35, Dragées
Galenic form
UEBT
ATC Code
G03HB01
Authorization status
Z
Dispensation category
B
First authorization
27/05/2004
Authorization expiration date
31/12/9999
IT number
07.09.0.
Domain
Human medicine
Field of application
Androgenisierungserscheinungen

Packaging details

Description (FR)
FEMINAC 35 drag 2 mg 21 pce
Description (DE)
FEMINAC 35 Drag 2 mg 21 Stk
Market launch
27/05/2004
Narcotic (BTM)
No

Other packaging sizes

FEMINAC 35 drag 2 mg 3x21 pce
3x21 DRG
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