PRONTOFLEX 10%
100MG/ML DRM SPR SOL 25ML
| SÚKL code | 0119940 |
|---|---|
| Name of the product | PRONTOFLEX 10% |
| _MA_MEDICATION_DETAIL_INFO_MED_NAME i | PRONTOFLEX 10% |
| Supplement | 100MG/ML DRM SPR SOL 25ML |
| Strenght | 100MG/ML |
| Pharmaceutical form | Cutaneous spray, solution |
| Package | 25ML |
| Route | Cutaneous use |
| Language of the pack | Czech |
| Wrap type | Pressurised container |
| Legal status | na lékařský předpis |
| Active substance | KETOPROFEN (KETOPROFENUM) |
| ATC group | M02AA10 |
| ATC group name | KETOPROFEN |
Marketing authorisation information
| Registration Number | 29/ 228/05-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. 10. 2020 |
| MA Holder | CYATHUS Exquirere Pharmaforschungs GmbH, Bisamberg |
| MA Holder country | RAKOUSKO |
| Actual MA holder | LERAM pharmaceuticals s.r.o., Brno |
| Actual MA holder country | ČESKÁ REPUBLIKA |
cz