PRENEWEL

4MG/1,25MG TBL NOB 28 II

SÚKL code 0126030
Name of the product PRENEWEL
_MA_MEDICATION_DETAIL_INFO_MED_NAME i PRENEWEL
Supplement 4MG/1,25MG TBL NOB 28 II
Strenght 4MG/1,25MG
Pharmaceutical form Tablet
Package 28 II
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance INDAPAMIDE (INDAPAMIDUM)
PERINDOPRIL TERT-BUTYLAMINE (PERINDOPRILUM ERBUMINUM)
ATC group C09BA04
ATC group name PERINDOPRIL A DIURETIKA
Doping Diuretika a ostatní maskovací látky (nelze pro léčbu sportovců použít vůbec). Bližší informace viz http://www.antidoping.cz/.

Marketing authorisation information

Registration Number 58/ 687/07-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. 10. 2018
MA Holder Krka Polska, Sp. z o.o., Varšava
MA Holder country POLSKO
Actual MA holder Krka, d.d., Novo mesto, Novo mesto
Actual MA holder country SLOVINSKO

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