FINASTERID AUROVITAS
5MG TBL FLM 60
SÚKL code | 0229629 |
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Name of the product | FINASTERID AUROVITAS |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | FINASTERID AUROVITAS |
Supplement | 5MG TBL FLM 60 |
Strenght | 5MG |
Pharmaceutical form | Film-coated tablet |
Package | 60 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance | FINASTERIDE (FINASTERIDUM) |
ATC group | G04CB01 |
ATC group name | FINASTERID |
Marketing authorisation information
Registration Number | 87/ 427/16-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state |
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. 04. 2020 |
MA Holder | Aurovitas Pharma Polska Sp. z o.o., Warszawa |
MA Holder country | POLSKO |
Actual MA holder | Aurovitas, spol. s r.o., Praha |
Actual MA holder country | ČESKÁ REPUBLIKA |