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KLABAX

500MG TBL FLM 14

SÚKL code 0219550
Name of the product KLABAX
_MA_MEDICATION_DETAIL_INFO_MED_NAME i KLABAX
Supplement 500MG TBL FLM 14
Strenght 500MG
Pharmaceutical form Film-coated tablet
Package 14
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance CLARITHROMYCIN (CLARITHROMYCINUM)
ATC group J01FA09
ATC group name KLARITHROMYCIN

Marketing authorisation information

Registration Number 15/ 222/03-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. 11. 2020
MA Holder Adamed Czech Republic, s. r. o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder Glenmark Pharmaceuticals s.r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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