AMLODIPINE/VALSARTAN HCS

5MG/320MG TBL FLM 60X1

SÚKL code 0226858
Name of the product AMLODIPINE/VALSARTAN HCS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i AMLODIPINE/VALSARTAN HCS
Supplement 5MG/320MG TBL FLM 60X1
Strenght 5MG/320MG
Pharmaceutical form Film-coated tablet
Package 60X1
Route Oral use
Language of the pack Czech
Wrap type
Legal status na lékařský předpis
Active substance AMLODIPINE BESILATE (AMLODIPINI BESILAS)
VALSARTAN (VALSARTANUM)
ATC group C09DB01
ATC group name VALSARTAN A AMLODIPIN

Marketing authorisation information

Registration Number 58/ 423/17-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Reference 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 30. 04. 2020
MA Holder HCS bvba, Edegem
MA Holder country BELGIE
Actual MA holder Krka, d.d., Novo mesto, Novo mesto
Actual MA holder country SLOVINSKO

Back to list