KEFLAVO
500MG TBL FLM 15
SÚKL code | 0228522 |
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Name of the product | KEFLAVO |
_MA_MEDICATION_DETAIL_INFO_MED_NAME i | KEFLAVO |
Supplement | 500MG TBL FLM 15 |
Strenght | 500MG |
Pharmaceutical form | Film-coated tablet |
Package | 15 |
Route | Oral use |
Language of the pack | Czech |
Wrap type | Blister |
Legal status | OTC medicinal products |
Active substance | MICRONIZED FLAVONOIDES (FLAVONOIDA MICRONISATA) |
ATC group | C05CA53 |
ATC group name | DIOSMIN, KOMBINACE |
Marketing authorisation information
Registration Number | 85/ 107/18-C |
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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. 01. 2022 |
MA Holder | Kern Pharma S.L., Terrasa (Barcelona) |
MA Holder country | ŠPANĚLSKO |
Actual MA holder | VIATRIS LIMITED, Dublin |
Actual MA holder country | IRSKO |