ZNOBACT

500MG TBL FLM 120

SÚKL code 0215118
Name of the product ZNOBACT 500 MG POTAHOVANÉ TABLETY
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ZNOBACT
Supplement 500MG TBL FLM 120
Strenght 500MG
Pharmaceutical form Film-coated tablet
Package 120
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance CEFUROXIME AXETIL (CEFUROXIMUM AXETILUM)
ATC group J01DC02
ATC group name CEFUROXIM

Marketing authorisation information

Registration Number 15/ 197/16-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. 08. 2017
MA Holder Sun Pharmaceutical Industries Europe B.V., Hoofddorp
MA Holder country NIZOZEMSKO
Actual MA holder Adamed Czech Republic, s. r. o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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