TELMISARTAN/AMLODIPIN TEVA
40MG/5MG TBL NOB 98
| SÚKL code | 0251731 |
|---|---|
| Name of the product | TELMISARTAN/AMLODIPIN TEVA |
| _MA_MEDICATION_DETAIL_INFO_MED_NAME i | TELMISARTAN/AMLODIPIN TEVA |
| Supplement | 40MG/5MG TBL NOB 98 |
| Strenght | 40MG/5MG |
| Pharmaceutical form | Tablet |
| Package | 98 |
| 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/ 438/20-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 | Teva B.V., Haarlem |
| MA Holder country | NIZOZEMSKO |
cz