KENACORT A 40 susp inj 200 mg/5ml flac 5 ml
7680329900453
CH-32990
H02AB08
07.07.24
1 / 3
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Details
- Product number
- 3299002
- CPT
- -
- Packaging group
- 1 x 5 mL
- Unit
- Durchstechflasche(n)
- Composition
- triamcinoloni acetonidum 200 mg, alcohol benzylicus 49.5 mg, carmellosum natricum, polysorbatum 80, natrii chloridum, acidum hydrochloridum ad pH, natrii hydroxidum ad pH, aqua ad iniectabile q.s. ad suspensionem pro 5 ml corresp. natrium 16.5 mg.
Articles (1)
Kenacort-A 40 200 mg/5 mL, Injektionssuspension
Injektionssuspension
1 x 5 mL
Official Swissmedic V2 data
Additional information from the official database
Detailed composition
| Substance | Quantity | Type | Category |
|---|---|---|---|
|
(N/A)
|
200.0 MG | Substance | Wirkstoff (Principe actif) |
|
(N/A)
|
49.5 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)
|
16.5 MG | Substance | HBESI |
Authorization holder
Dermapharm AG
6331 Hünenberg
Authorization information
- Swissmedic authorization number
- 32990
- Drug name
- Kenacort-A 40, Injektionssuspension
- Galenic form
- SUPA
- ATC Code
- H02AB08
- Authorization status
- Z
- Dispensation category
- B
- First authorization
- 12/07/1967
- Authorization expiration date
- 31/12/9999
- IT number
- 07.07.24
- Domain
- Human medicine
Packaging details
- Description (FR)
- KENACORT A 40 susp inj 200 mg/5ml flac 5 ml
- Description (DE)
- KENACORT A 40 Inj Susp 200 mg/5ml Durchstf 5 ml
- Market launch
- 02/04/2015
- Narcotic (BTM)
- No