LORISTA
50MG TBL FLM 20
SÚKL code | 0107771 |
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Name of the product | LORISTA |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | LORISTA |
Supplement | 50MG TBL FLM 20 |
Strenght | 50MG |
Pharmaceutical form | Film-coated tablet |
Package | 20 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance | LOSARTAN POTASSIUM (LOSARTANUM KALICUM) |
ATC group | C09CA01 |
ATC group name | LOSARTAN |
Marketing authorisation information
Registration Number | 58/ 116/02-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Reference member state |
MA status | R - active MA/authorised medicinal product |
MA Holder | Krka, d.d., Novo mesto, Novo mesto |
MA Holder country | SLOVINSKO |