ZOREM
10MG TBL NOB 50X1
SÚKL code | 0192245 |
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Name of the product | ZOREM |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | ZOREM |
Supplement | 10MG TBL NOB 50X1 |
Strenght | 10MG |
Pharmaceutical form | Tablet |
Package | 50X1 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | |
Legal status | na lékařský předpis |
Active substance | AMLODIPINE BESILATE (AMLODIPINI BESILAS) |
ATC group | C08CA01 |
ATC group name | AMLODIPIN |
Marketing authorisation information
Registration Number | 83/ 375/01-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 | 28. 02. 2022 |
MA Holder | Pfizer, spol. s r.o., Praha |
MA Holder country | ČESKÁ REPUBLIKA |
Actual MA holder | Upjohn EESV, Capelle aan den IJssel |
Actual MA holder country | NIZOZEMSKO |