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RUNAPLAX

20MG TBL FLM 100 III

SÚKL code 0229086
Name of the product RUNAPLAX
_MA_MEDICATION_DETAIL_INFO_MED_NAME i RUNAPLAX
Supplement 20MG TBL FLM 100 III
Strenght 20MG
Pharmaceutical form Film-coated tablet
Package 100 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/ 905/16-C
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

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