BATRAFEN
10MG/ML DRM SOL 10ML
SÚKL code | 0076151 |
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Name of the product | BATRAFEN |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | BATRAFEN |
Supplement | 10MG/ML DRM SOL 10ML |
Strenght | 10MG/ML |
Pharmaceutical form | Cutaneous solution |
Package | 10ML |
Route | Cutaneous use |
Language of the pack | Czech |
Wrap type | Dropper container |
Legal status | na lékařský předpis |
Active substance | CICLOPIROX OLAMINE (CICLOPIROXUM OLAMINUM) |
ATC group | D01AE14 |
ATC group name | CIKLOPIROX |
Marketing authorisation information
Registration Number | 26/ 465/95-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. 06. 2022 |
MA Holder | sanofi-aventis, s.r.o., Praha |
MA Holder country | ČESKÁ REPUBLIKA |
Actual MA holder | Zentiva, k.s., Praha |
Actual MA holder country | ČESKÁ REPUBLIKA |