ZOLETORV
10MG/10MG TBL FLM 10
| SÚKL code | 0233457 |
|---|---|
| Name of the product | ZOLETORV |
| _MA_MEDICATION_DETAIL_INFO_MED_NAME i | ZOLETORV |
| Supplement | 10MG/10MG TBL FLM 10 |
| Strenght | 10MG/10MG |
| Pharmaceutical form | Film-coated tablet |
| Package | 10 |
| Route | Oral use |
| Language of the pack | Czech |
| Wrap type | Blister |
| Legal status | na lékařský předpis |
| Active substance |
ATORVASTATIN CALCIUM TRIHYDRATE (ATORVASTATINUM CALCICUM TRIHYDRICUM) EZETIMIBE (EZETIMIBUM) |
| ATC group | C10BA05 |
| ATC group name | ATORVASTATIN A EZETIMIB |
Marketing authorisation information
| Registration Number | 31/ 403/14-C |
|---|---|
| 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. 10. 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 |
cz