ULIPRISTAL Sandoz cpr pell 30 mg
7680687990011
CH-68799
G03AD02
09.02.1.
1 / 3
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Details
- Product number
- 6879901
- CPT
- -
- Packaging group
- 1
- Unit
- Tablette(n)
- Composition
- ulipristalii acetas 30 mg, lactosum monohydricum 240 mg, amylum pregelificatum, carboxymethylamylum natricum A, magnesii stearas, Überzug: hypromellosum, hydroxypropylcellulosum, acidum stearicum, talcum, E 171, pro compresso obducto, natrium max. 0.5 mg.
Articles (1)
Ulipristal Sandoz, Filmtablette
Filmtablette
1
Official Swissmedic V2 data
Additional information from the official database
Official medical documents
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
(N/A)
|
30.0 MG | Substance | Wirkstoff (Principe actif) |
|
(N/A)
|
240.0 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 | HNIDK |
|
(N/A)
|
- | Substance | FNIDK |
|
(N/A)
|
- | Substance | HBESI |
Authorization holder
Sandoz Pharmaceuticals AG
6343 Risch
Authorization information
- Swissmedic authorization number
- 68799
- Drug name
- Ulipristal Sandoz, Filmtablette
- Galenic form
- FILM
- ATC Code
- G03AD02
- Authorization status
- Z
- Dispensation category
- B
- First authorization
- 30/03/2023
- Authorization expiration date
- 29/03/2028
- IT number
- 09.02.1.
- Domain
- Human medicine
Packaging details
- Description (FR)
- ULIPRISTAL Sandoz cpr pell 30 mg
- Description (DE)
- ULIPRISTAL Sandoz Filmtabl 30 mg
- Market launch
- 30/03/2023
- Narcotic (BTM)
- No