ATORVASTATIN MYLAN

40MG TBL FLM 56 II

SÚKL code 0202193
Name of the product ATORVASTATIN MYLAN
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ATORVASTATIN MYLAN
Supplement 40MG TBL FLM 56 II
Strenght 40MG
Pharmaceutical form Film-coated tablet
Package 56 II
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance ATORVASTATIN CALCIUM TRIHYDRATE (ATORVASTATINUM CALCICUM TRIHYDRICUM)
ATC group C10AA05
ATC group name ATORVASTATIN

Marketing authorisation information

Registration Number 31/ 891/10-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 28. 02. 2019
MA Holder Generics [UK] Limited, Potters Bar
MA Holder country VELKÁ BRITÁNIE
Actual MA holder Mylan Ireland Limited, Dublin
Actual MA holder country IRSKO

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