TEVETEN
600MG TBL FLM 56
SÚKL code | 0215565 |
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Name of the product | TEVETEN 600 MG |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | TEVETEN |
Supplement | 600MG TBL FLM 56 |
Strenght | 600MG |
Pharmaceutical form | Film-coated tablet |
Package | 56 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance | EPROSARTAN MESILATE (EPROSARTANI MESILAS) |
ATC group | C09CA02 |
ATC group name | EPROSARTAN |
Marketing authorisation information
Registration Number | 58/ 022/01-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. 10. 2018 |
MA Holder | BGP Products B.V., Hoofddorp |
MA Holder country | NIZOZEMSKO |
Actual MA holder | Mylan IRE Healthcare Limited, Dublin |
Actual MA holder country | IRSKO |