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ENDIARON

250MG TBL FLM 40

SÚKL code 0229192
Name of the product ENDIARON
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ENDIARON
Supplement 250MG TBL FLM 40
Strenght 250MG
Pharmaceutical form Film-coated tablet
Package 40
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status OTC medicinal products
Active substance CHLOROXINE (CLOROXINUM)
ATC group A07AX
ATC group name JINÁ STŘEVNÍ ANTIINFEKTIVA

Marketing authorisation information

Registration Number 42/ 101/74-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 31. 12. 2021
MA Holder sanofi-aventis, s.r.o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder Opella Healthcare Czech s.r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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