EXODERIL
10MG/ML DRM SOL 1X30ML
| SÚKL code | 0208317 |
|---|---|
| Name of the product | EXODERIL |
| _MA_MEDICATION_DETAIL_INFO_MED_NAME i | EXODERIL |
| Supplement | 10MG/ML DRM SOL 1X30ML |
| Strenght | 10MG/ML |
| Pharmaceutical form | Cutaneous solution |
| Package | 1X30ML |
| Route | Cutaneous use |
| Language of the pack | Czech |
| Wrap type | Dropper container |
| Legal status | OTC medicinal products |
| Active substance | NEFTIFINE HYDROCHLORIDE (NAFTIFINI HYDROCHLORIDUM) |
| ATC group | D01AE22 |
| ATC group name | NAFTIFIN |
Marketing authorisation information
| Registration Number | 26/1321/97-C |
|---|---|
| Type of MA | National |
| MA status | B - medicinal product after change, may be placed on the market for the period of 6 months (Placed on the market till) and used until expiration, not later than till the end of validity of the marketing authorisation (Valid till) |
| Placed on the market till | 31. 03. 2022 |
| MA Holder | Sandoz GmbH, Kundl |
| MA Holder country | RAKOUSKO |
| Actual MA holder | Sandoz GmbH, Kundl |
| Actual MA holder country | RAKOUSKO |
cz