TERFIMED
250MG TBL NOB 8 II
SÚKL code | 0199686 |
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Name of the product | TERFIMED |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | TERFIMED |
Supplement | 250MG TBL NOB 8 II |
Strenght | 250MG |
Pharmaceutical form | Tablet |
Package | 8 II |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance | TERBINAFINE HYDROCHLORIDE (TERBINAFINI HYDROCHLORIDUM) |
ATC group | D01BA02 |
ATC group name | TERBINAFIN |
Marketing authorisation information
Registration Number | 26/ 489/06-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state |
MA status | R - active MA/authorised medicinal product |
MA Holder | PRO.MED.CS Praha a.s. |
MA Holder country | ČESKÁ REPUBLIKA |