DURACEF
500MG CPS DUR 12
SÚKL code | 0199803 |
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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 |
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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 | 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 |