Drovelis 3 mg/14.2 mg, Filmtabletten
7680682280049
CH-68228
G03AA
09.02.1.
1 / 3
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Details
- Product number
- 6822801
- CPT
- -
- Packaging group
- 13 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
13 x 28
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
II
|
67.66 MG | Substance | HBESI |
|
I
|
15.0 MG | Substance | WIZUS |
|
II
|
- | Substance | HNIDK |
|
I
|
14.2 MG | Substance | Wirkstoff (Principe actif) |
|
II
|
- | Substance | HNIDK |
|
I
|
3.0 MG | Substance | Wirkstoff (Principe actif) |
|
I
|
39.9 MG | Substance | HBESI |
|
I
|
- | Substance | HNIDK |
|
II
|
- | Substance | HNIDK |
|
II
|
- | Substance | HNIDK |
|
I
|
0.313 MG | Substance | HBESI |
|
II
|
- | Substance | HNIDK |
|
I
|
- | Substance | HNIDK |
|
II
|
- | Substance | HNIDK |
|
I
|
- | Substance | HNIDK |
|
I
|
- | Substance | HNIDK |
|
II
|
- | Substance | FNIDK |
|
I
|
- | Substance | HNIDK |
|
I
|
- | Substance | HNIDK |
|
I
|
- | Substance | HNIDK |
|
I
|
- | Substance | HNIDK |
|
I
|
- | Substance | FNIDK |
|
I
|
- | 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
- G03AA
- 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
Packaging details
- Description (FR)
- DROVELIS cpr pell 3 mg/14.2 mg 13 x 28 pce
- Description (DE)
- DROVELIS Filmtabl 3 mg/14.2 mg 13 x 28 Stk
- Narcotic (BTM)
- No