BRUFEN
400MG TBL FLM 50 I
| SÚKL code | 0254405 |
|---|---|
| Name of the product | BRUFEN |
| _MA_MEDICATION_DETAIL_INFO_MED_NAME i | BRUFEN |
| Supplement | 400MG TBL FLM 50 I |
| Strenght | 400MG |
| Pharmaceutical form | Film-coated tablet |
| Package | 50 I |
| Route | Oral use |
| Language of the pack | Czech |
| Wrap type | Blister |
| Legal status | OTC medicinal products |
| Active substance | IBUPROFEN (IBUPROFENUM) |
| ATC group | M01AE01 |
| ATC group name | IBUPROFEN |
Marketing authorisation information
| Registration Number | 29/ 390/92-S/C |
|---|---|
| Type of MA | National |
| 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 | 30. 06. 2023 |
| MA Holder | Mylan IRE Healthcare Limited, Dublin |
| MA Holder country | IRSKO |
| Actual MA holder | VIATRIS HEALTHCARE LIMITED, Dublin |
| Actual MA holder country | IRSKO |
cz