ROSUVASTATIN AUROVITAS

10MG TBL FLM 500

SÚKL code 0229988
Name of the product ROSUVASTATIN AUROVITAS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ROSUVASTATIN AUROVITAS
Supplement 10MG TBL FLM 500
Strenght 10MG
Pharmaceutical form Film-coated tablet
Package 500
Route Oral use
Language of the pack Czech
Wrap type Tablet container
Legal status na lékařský předpis
Active substance ROSUVASTATIN CALCIUM (ROSUVASTATINUM CALCICUM)
ATC group C10AA07
ATC group name ROSUVASTATIN

Marketing authorisation information

Registration Number 31/ 111/13-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. 05. 2020
MA Holder Aurovitas Pharma Polska Sp. z o.o., Warszawa
MA Holder country POLSKO
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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