KALETRA 200/50 cpr pellic 200 mg 120 pce
7680575550013
CH-57555
J05AR10
08.03.0.
Active substances:
1 / 2
Fiches Amavita / Sun Store / Coop Vitality
Details
- Product number
- 5755501
- CPT
- -
- Packaging group
- 120
- Unit
- Tablette(n)
- Composition
- lopinavirum 200 mg, ritonavirum 50 mg, copovidonum K 28, sorbitani lauras, silica colloidalis anhydrica, natrii stearylis fumaras, Überzug: hypromellosum, macrogolum 400, hydroxypropylcellulosum, talcum, macrogolum 3350, polysorbatum 80, silica colloidalis anhydrica, E 171, E 172 (rubrum), pro compresso obducto corresp. natrium 724 µg.
Articles (1)
Kaletra 200/50, Filmtabletten
Filmtabletten
120
Official Swissmedic V2 data
Additional information from the official database
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
lopinavirum
|
200.0 MG | Substance | Wirkstoff (Principe actif) |
|
ritonavirum
|
50.0 MG | Substance | Wirkstoff (Principe actif) |
|
copovidonum K 28
|
- | Substance | HNIDK |
|
sorbitani lauras
|
- | Substance | HNIDK |
|
silica colloidalis anhydrica
|
- | Substance | HNIDK |
|
natrii stearylis fumaras
|
- | Substance | HNIDK |
|
hypromellosum
|
- | Substance | HNIDK |
|
macrogolum 400
|
- | Substance | Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration) |
|
hydroxypropylcellulosum
|
- | Substance | HNIDK |
|
talcum
|
- | Substance | HNIDK |
|
macrogolum 3350
|
- | Substance | HNIDK |
|
polysorbatum 80
|
- | Substance | HNIDK |
|
silica colloidalis anhydrica
|
- | Substance | HNIDK |
|
E 171
|
- | Substance | HNIDK |
|
E 172 (rubrum)
|
- | Substance | FTODK |
|
natrium
|
724.0 UG | Substance | HBESI |
Reimbursement information
Public price
CHF 443.10
Specialties list
Yes
Generic
No
SL addition date:
01/12/2006
Authorization holder
AbbVie AG
6330 Cham
Authorization information
- Swissmedic authorization number
- 57555
- Drug name
- Kaletra, Filmtabletten
- Galenic form
- FILM
- ATC Code
- J05AR10
- Authorization status
- Z
- Dispensation category
- A
- First authorization
- 22/08/2006
- Authorization expiration date
- 01/10/2026
- IT number
- 08.03.0.
- Domain
- Human medicine
Packaging details
- Description (FR)
- KALETRA 200/50 cpr pellic 200 mg 120 pce
- Description (DE)
- KALETRA 200/50 Filmtabl 200 mg 120 Stk
- Market launch
- 22/08/2006
- Market withdrawal
- 30/09/2026
- Narcotic (BTM)
- No