EZETROL
10MG TBL NOB 300X1 III
SÚKL code | 0008942 |
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Name of the product | EZETROL |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | EZETROL |
Supplement | 10MG TBL NOB 300X1 III |
Strenght | 10MG |
Pharmaceutical form | Tablet |
Package | 300X1 III |
Route | Oral use |
Wrap type | |
Legal status | na lékařský předpis |
Active substance | EZETIMIBE (EZETIMIBUM) |
ATC group | C10AX09 |
ATC group name | EZETIMIB |
Marketing authorisation information
Registration Number | 31/ 267/03-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 | 31. 01. 2022 |
MA Holder | Merck Sharp & Dohme B.V., Haarlem |
MA Holder country | NIZOZEMSKO |
Actual MA holder | N.V. Organon, Oss |
Actual MA holder country | NIZOZEMSKO |