SORAFENIB VIATRIS
200MG TBL FLM 112
SÚKL code | 0267536 |
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Name of the product | SORAFENIB VIATRIS |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | SORAFENIB VIATRIS |
Supplement | 200MG TBL FLM 112 |
Strenght | 200MG |
Pharmaceutical form | Film-coated tablet |
Package | 112 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance | SORAFENIB TOSILATE (SORAFENIBI TOSILAS) |
ATC group | L01EX02 |
ATC group name | SORAFENIB |
Marketing authorisation information
Registration Number | 44/ 448/19-C |
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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. 10. 2023 |
MA Holder | Mylan Ireland Limited, Dublin |
MA Holder country | IRSKO |
Actual MA holder | VIATRIS LIMITED, Dublin |
Actual MA holder country | IRSKO |