TELMISARTAN/HYDROCHLOROTHIAZID RATIOPHARM
80MG/12,5MG TBL NOB 50X1
| SÚKL code | 0189900 |
|---|---|
| Name of the product | TELMISARTAN/HYDROCHLOROTHIAZID RATIOPHARM |
| _MA_MEDICATION_DETAIL_INFO_MED_NAME i | TELMISARTAN/HYDROCHLOROTHIAZID RATIOPHARM |
| Supplement | 80MG/12,5MG TBL NOB 50X1 |
| Strenght | 80MG/12,5MG |
| Pharmaceutical form | Tablet |
| Package | 50X1 |
| Route | Oral use |
| Language of the pack | Czech |
| Wrap type | |
| Legal status | na lékařský předpis |
| Active substance |
HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDUM) TELMISARTAN (TELMISARTANUM) |
| ATC group | C09DA07 |
| ATC group name | TELMISARTAN A DIURETIKA |
| Doping | Diuretika a maskovací látky (nelze pro léčbu sportovců použít vůbec). Bližší informace viz www.antidoping.cz/cs/zakazane-leky |
Marketing authorisation information
| Registration Number | 58/ 121/14-C |
|---|---|
| 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 | ratiopharm GmbH, Ulm |
| MA Holder country | NĚMECKO |
cz