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DUOMOX

1000MG TBL SUS 14

SÚKL code 0019751
Name of the product DUOMOX
_MA_MEDICATION_DETAIL_INFO_MED_NAME i DUOMOX
Supplement 1000MG TBL SUS 14
Strenght 1000MG
Pharmaceutical form Dispersible tablet
Package 14
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance AMOXICILLIN TRIHYDRATE (AMOXICILLINUM TRIHYDRICUM)
ATC group J01CA04
ATC group name AMOXICILIN

Marketing authorisation information

Registration Number 15/ 270/93-E/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 30. 11. 2022
MA Holder Astellas Pharma s.r.o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder CHEPLAPHARM Arzneimittel GmbH, Greifswald
Actual MA holder country NĚMECKO

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