DUOMOX
500MG TBL SUS 20
SÚKL code | 0062050 |
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Name of the product | DUOMOX |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | DUOMOX |
Supplement | 500MG TBL SUS 20 |
Strenght | 500MG |
Pharmaceutical form | Dispersible tablet |
Package | 20 |
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-C/C |
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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 |