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KEFLAVO

500MG TBL FLM 20

SÚKL code 0228523
Name of the product KEFLAVO
_MA_MEDICATION_DETAIL_INFO_MED_NAME i KEFLAVO
Supplement 500MG TBL FLM 20
Strenght 500MG
Pharmaceutical form Film-coated tablet
Package 20
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
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 Mylan Ireland Limited, Dublin
Actual MA holder country IRSKO

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