DROVELIS cpr pell 3 mg/14.2 mg 28 pce

7680682280018 CH-68228 G03AA18 09.02.1.

Active substances:

DROVELIS cpr pell 3 mg/14.2 mg 28 pce
Fiches Amavita / Sun Store / Coop Vitality

Details

Product number
6822801
CPT
-
Packaging group
1 x 28
Unit
Tablette(n)
Composition
I) Wirkstoffhaltige Tablette: estetrolum monohydricum 15.0 mg corresp. estetrolum 14.2 mg, drospirenonum 3.0 mg, lactosum monohydricum 39.9 mg, carboxymethylamylum natricum A corresp. natrium 0.313 mg, maydis amylum, povidonum K 30, magnesii stearas, Überzug: hypromellosum, hydroxypropylcellulosum, talcum, gossypii oleum hydrogenatum, E 171, E 172 (rubrum), pro compresso obducto. II) Placebo: lactosum monohydricum 67.66 mg, maydis amylum, magnesii stearas, Überzug: hypromellosum, hydroxypropylcellulosum, talcum, gossypii oleum hydrogenatum, E 171, pro compresso obducto.

Articles (1)

Drovelis 3 mg/14.2 mg, Filmtabletten
Filmtabletten
1 x 28
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Official Swissmedic V2 data

Additional information from the official database

Official medical documents

Patient information leaflet
Allemand
21/02/2026
Patient information leaflet
Français
21/02/2026
Patient information leaflet
Italien
21/02/2026
Professional SmPC
Allemand
18/02/2026
Professional SmPC
Français
18/02/2026
Professional SmPC
Italien
18/02/2026

Detailed composition

Substance Quantity Type Category
lactosum monohydricum
67.66 MG Substance HBESI
estetrolum monohydricum
15.0 MG Substance WIZUS
maydis amylum
- Substance HNIDK
estetrolum
14.2 MG Substance Wirkstoff (Principe actif)
magnesii stearas
- Substance HNIDK
drospirenonum
3.0 MG Substance Wirkstoff (Principe actif)
lactosum monohydricum
39.9 MG Substance HBESI
carboxymethylamylum natricum A
- Substance HNIDK
hypromellosum
- Substance HNIDK
hydroxypropylcellulosum
- Substance HNIDK
natrium
0.313 MG Substance HBESI
talcum
- Substance HNIDK
maydis amylum
- Substance HNIDK
gossypii oleum hydrogenatum
- Substance HNIDK
povidonum K 30
- Substance HNIDK
magnesii stearas
- Substance HNIDK
E 171
- Substance FNIDK
hypromellosum
- Substance HNIDK
hydroxypropylcellulosum
- Substance HNIDK
talcum
- Substance HNIDK
gossypii oleum hydrogenatum
- Substance HNIDK
E 171
- Substance FNIDK
E 172 (rubrum)
- Substance FTODK

Authorization holder

Gedeon Richter (Schweiz) AG

1202 Genève

Authorization information

Swissmedic authorization number
68228
Drug name
Drovelis, Filmtabletten
Galenic form
FILM
ATC Code
G03AA18
Authorization status
Z
Dispensation category
B
First authorization
05/05/2022
Authorization expiration date
04/05/2027
IT number
09.02.1.
Domain
Human medicine
Field of application
Hormonales Kontrazeptivum

Packaging details

Description (FR)
DROVELIS cpr pell 3 mg/14.2 mg 28 pce
Description (DE)
DROVELIS Filmtabl 3 mg/14.2 mg 28 Stk
Market launch
05/05/2022
Narcotic (BTM)
No

Other packaging sizes

DROVELIS cpr pell 3 mg/14.2 mg 3 x 28 pce
3 x 28 TABL
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DROVELIS cpr pell 3 mg/14.2 mg 6 x 28 pce
6 x 28 TABL
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DROVELIS cpr pell 3 mg/14.2 mg 13 x 28 pce
13 x 28 TABL
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