SORTIS
10MG TBL FLM 28
SÚKL code | 0187483 |
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Name of the product | SORTIS |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | SORTIS |
Supplement | 10MG TBL FLM 28 |
Strenght | 10MG |
Pharmaceutical form | Film-coated tablet |
Package | 28 |
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/ 233/99-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 | 30. 04. 2022 |
MA Holder | Pfizer, spol. s r.o., Praha |
MA Holder country | ČESKÁ REPUBLIKA |
Actual MA holder | Upjohn EESV, Capelle aan den IJssel |
Actual MA holder country | NIZOZEMSKO |