RUNAPLAX
10MG TBL FLM 20 III
SÚKL code | 0229061 |
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Name of the product | RUNAPLAX |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | RUNAPLAX |
Supplement | 10MG TBL FLM 20 III |
Strenght | 10MG |
Pharmaceutical form | Film-coated tablet |
Package | 20 III |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance | RIVAROXABAN (RIVAROXABANUM) |
ATC group | B01AF01 |
ATC group name | RIVAROXABAN |
Marketing authorisation information
Registration Number | 16/ 903/16-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 | Sandoz s.r.o., Praha |
MA Holder country | ČESKÁ REPUBLIKA |