CEFZIL

500MG TBL FLM 20

SÚKL code 0199797
Name of the product CEFZIL 500 MG
_MA_MEDICATION_DETAIL_INFO_MED_NAME i CEFZIL
Supplement 500MG TBL FLM 20
Strenght 500MG
Pharmaceutical form Film-coated tablet
Package 20
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance CEFPROZIL MONOHYDRATE (CEFPROZILUM MONOHYDRICUM)
ATC group J01DC10
ATC group name CEFPROZIL

Marketing authorisation information

Registration Number 15/ 757/99-C
Type of MA National
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. 2021
MA Holder PharmaSwiss Česká republika s.r.o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder Bausch Health Ireland Limited, Dublin
Actual MA holder country IRSKO

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