IBALGIN

600MG TBL FLM 30

SÚKL code 0207900
Name of the product IBALGIN
_MA_MEDICATION_DETAIL_INFO_MED_NAME i IBALGIN
Supplement 600MG TBL FLM 30
Strenght 600MG
Pharmaceutical form Film-coated tablet
Package 30
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance IBUPROFEN (IBUPROFENUM)
ATC group M01AE01
ATC group name IBUPROFEN

Marketing authorisation information

Registration Number 29/1235/97-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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