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PERINDOPRIL/AMLODIPIN MYLAN

8MG/10MG TBL NOB 30

SÚKL code 0246580
Name of the product PERINDOPRIL/AMLODIPIN MYLAN
_MA_MEDICATION_DETAIL_INFO_MED_NAME i PERINDOPRIL/AMLODIPIN MYLAN
Supplement 8MG/10MG TBL NOB 30
Strenght 8MG/10MG
Pharmaceutical form Tablet
Package 30
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance AMLODIPINE BESILATE (AMLODIPINI BESILAS)
PERINDOPRIL TERT-BUTYLAMINE (PERINDOPRILUM ERBUMINUM)
ATC group C09BB04
ATC group name PERINDOPRIL A AMLODIPIN

Marketing authorisation information

Registration Number 58/ 406/19-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 31. 05. 2022
MA Holder Mylan Ireland Limited, Dublin
MA Holder country IRSKO
Actual MA holder VIATRIS LIMITED, Dublin
Actual MA holder country IRSKO

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