BRUFEN
600MG GRA EFF 20
SÚKL code | 0234203 |
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Name of the product | BRUFEN |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | BRUFEN |
Supplement | 600MG GRA EFF 20 |
Strenght | 600MG |
Pharmaceutical form | Effervescent granules |
Package | 20 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Sachet |
Legal status | na lékařský předpis |
Active substance | IBUPROFEN (IBUPROFENUM) |
ATC group | M01AE01 |
ATC group name | IBUPROFEN |
Marketing authorisation information
Registration Number | 29/ 655/08-C |
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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 |