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SORAFENIB VIATRIS

200MG TBL FLM 112

SÚKL code 0267536
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
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

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