ECRITEN
100MG TBL FLM 4
| SÚKL code | 0202883 |
|---|---|
| Name of the product | ECRITEN 100 MG POTAHOVANÉ TABLETY |
| _MA_MEDICATION_DETAIL_INFO_MED_NAME i | ECRITEN |
| Supplement | 100MG TBL FLM 4 |
| Strenght | 100MG |
| Pharmaceutical form | Film-coated tablet |
| Package | 4 |
| Route | Oral use |
| Language of the pack | Czech |
| Wrap type | Blister |
| Legal status | na lékařský předpis |
| Active substance | SILDENAFIL CITRATE (SILDENAFILI CITRAS) |
| ATC group | G04BE03 |
| ATC group name | SILDENAFIL |
Marketing authorisation information
| Registration Number | 83/ 654/10-C |
|---|---|
| Type of MA | A mutual recognition procedure (MRP, DCP), where CZ is Reference 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. 07. 2020 |
| MA Holder | PharmaSwiss Česká republika s.r.o., Praha |
| MA Holder country | ČESKÁ REPUBLIKA |
| Actual MA holder | Bausch Health Ireland Limited, Dublin |
| Actual MA holder country | IRSKO |
cz