LOSARTAN AUROBINDO

50MG TBL FLM 28

SÚKL code 0208777
Name of the product LOSARTAN AUROBINDO 50 MG POTAHOVANÉ TABLETY
_MA_MEDICATION_DETAIL_INFO_MED_NAME i LOSARTAN AUROBINDO
Supplement 50MG TBL FLM 28
Strenght 50MG
Pharmaceutical form Film-coated tablet
Package 28
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/ 134/15-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state
MA status B - medicinal product after change, may be placed on the market for the period of 6 months (Placed on the market till) and used until expiration, not later than till the end of validity of the marketing authorisation (Valid till)
Placed on the market till 28. 02. 2019
MA Holder Aurobindo Pharma (Malta) Limited, Floriana
MA Holder country MALTA
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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