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DURACEF

500MG CPS DUR 12

SÚKL code 0199803
Name of the product DURACEF
_MA_MEDICATION_DETAIL_INFO_MED_NAME i DURACEF
Supplement 500MG CPS DUR 12
Strenght 500MG
Pharmaceutical form Capsule, hard
Package 12
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance CEFADROXIL MONOHYDRATE (CEFADROXILUM MONOHYDRICUM)
ATC group J01DB05
ATC group name CEFADROXIL

Marketing authorisation information

Registration Number 15/ 009/84-B/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. 08. 2020
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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