EXOROLAK
50MG/ML LAC UGC 1X2,5ML
| SÚKL code | 0220863 |
|---|---|
| Name of the product | EXOROLAK |
| _MA_MEDICATION_DETAIL_INFO_MED_NAME i | EXOROLAK |
| Supplement | 50MG/ML LAC UGC 1X2,5ML |
| Strenght | 50MG/ML |
| Pharmaceutical form | Medicated nail lacquer |
| Package | 1X2,5ML |
| Route | Cutaneous use |
| Language of the pack | Czech |
| Wrap type | Bottle |
| Legal status | na lékařský předpis |
| Active substance | AMOROLFINE HYDROCHLORIDE (AMOROLFINI HYDROCHLORIDUM) |
| ATC group | D01AE16 |
| ATC group name | AMOROLFIN |
Marketing authorisation information
| Registration Number | 26/ 010/17-C |
|---|---|
| Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state |
| 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. 01. 2020 |
| MA Holder | Laboratoires Gerda, Paris |
| MA Holder country | FRANCIE |
| Actual MA holder | Sandoz s.r.o., Praha |
| Actual MA holder country | ČESKÁ REPUBLIKA |
cz