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LORISTA

12,5MG TBL FLM 21

SÚKL code 0107178
Name of the product LORISTA
_MA_MEDICATION_DETAIL_INFO_MED_NAME i LORISTA
Supplement 12,5MG TBL FLM 21
Strenght 12,5MG
Pharmaceutical form Film-coated tablet
Package 21
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/ 393/06-C
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

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