CO-AMOXI Mepha cpr pell 1000 mg 20 pce
7680557300049
CH-55730
J01CR02
08.01.93
Active substances:
1 / 3
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Details
- Product number
- 5573001
- CPT
- -
- Packaging group
- 20
- Unit
- Tablette(n)
- Composition
- amoxicillinum anhydricum 875 mg ut amoxicillinum trihydricum, acidum clavulanicum 125 mg ut kalii clavulanas, silica colloidalis anhydrica, magnesii stearas, talcum, povidonum K 25, cellulosum microcristallinum, crospovidonum, Überzug: triethylis citras, hypromellosum, ethylcellulosum, alcohol cetylicus, natrii laurilsulfas, E 171, pro compresso obducto corresp. natrium 72 µg.
Articles (1)
Co-Amoxi-Mepha 1000 mg, Filmtabletten
Filmtabletten
20
Official Swissmedic V2 data
Additional information from the official database
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
amoxicillinum anhydricum
|
875.0 MG | Substance | Wirkstoff (Principe actif) |
|
amoxicillinum trihydricum
|
- | Substance | WIZUS |
|
acidum clavulanicum
|
125.0 MG | Substance | Wirkstoff (Principe actif) |
|
kalii clavulanas
|
- | Substance | WIZUS |
|
silica colloidalis anhydrica
|
- | Substance | HNIDK |
|
magnesii stearas
|
- | Substance | HNIDK |
|
talcum
|
- | Substance | HNIDK |
|
povidonum K 25
|
- | Substance | HNIDK |
|
cellulosum microcristallinum
|
- | Substance | HNIDK |
|
crospovidonum
|
- | Substance | HNIDK |
|
triethylis citras
|
- | Substance | HNIDK |
|
hypromellosum
|
- | Substance | HNIDK |
|
ethylcellulosum
|
- | Substance | HNIDK |
|
alcohol cetylicus
|
- | Substance | HNIDK |
|
natrii laurilsulfas
|
- | Substance | Hilfsstoff ohne Deklarationspflicht (Excipient sans obligation de déclaration) |
|
E 171
|
- | Substance | FNIDK |
|
natrium
|
72.0 UG | Substance | HBESI |
Reimbursement information
Public price
CHF 34.60
Specialties list
Yes
Generic
Yes
SL addition date:
01/04/2002
Authorization holder
Mepha Pharma AG
4051 Basel
Authorization information
- Swissmedic authorization number
- 55730
- Drug name
- Co-Amoxi-Mepha 1000 mg, Filmtabletten
- Galenic form
- FILM
- ATC Code
- J01CR02
- Authorization status
- Z
- Dispensation category
- A
- First authorization
- 10/09/2001
- Authorization expiration date
- 31/12/9999
- IT number
- 08.01.93
- Domain
- Human medicine
Packaging details
- Description (FR)
- CO-AMOXI Mepha cpr pell 1000 mg 20 pce
- Description (DE)
- CO-AMOXI Mepha Filmtabl 1000 mg 20 Stk
- Market launch
- 10/09/2001
- Narcotic (BTM)
- No