TEZEFORT
80MG/10MG TBL NOB 14
SÚKL code | 0206210 |
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Name of the product | TEZEFORT |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | TEZEFORT |
Supplement | 80MG/10MG TBL NOB 14 |
Strenght | 80MG/10MG |
Pharmaceutical form | Tablet |
Package | 14 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | na lékařský předpis |
Active substance |
AMLODIPINE BESILATE (AMLODIPINI BESILAS) TELMISARTAN (TELMISARTANUM) |
ATC group | C09DB04 |
ATC group name | TELMISARTAN A AMLODIPIN |
Marketing authorisation information
Registration Number | 58/ 411/15-C |
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Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Reference member state |
MA status | R - active MA/authorised medicinal product |
MA Holder | Zentiva, k.s., Praha |
MA Holder country | ČESKÁ REPUBLIKA |