ATORDAPIN
10MG/10MG TBL FLM 90
SÚKL code | 0189462 |
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Name of the product | ATORDAPIN |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | ATORDAPIN |
Supplement | 10MG/10MG TBL FLM 90 |
Strenght | 10MG/10MG |
Pharmaceutical form | Film-coated tablet |
Package | 90 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance |
AMLODIPINE BESILATE (AMLODIPINI BESILAS) ATORVASTATIN CALCIUM TRIHYDRATE (ATORVASTATINUM CALCICUM TRIHYDRICUM) |
ATC group | C10BX03 |
ATC group name | ATORVASTATIN A AMLODIPIN |
Marketing authorisation information
Registration Number | 83/ 240/13-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state |
MA status | R - active MA/authorised medicinal product |
MA Holder | Krka, d.d., Novo mesto, Novo mesto |
MA Holder country | SLOVINSKO |