IBALGIN 400

400MG TBL FLM 36

SÚKL code 0162673
Name of the product IBALGIN 400
_MA_MEDICATION_DETAIL_INFO_MED_NAME i IBALGIN 400
Supplement 400MG TBL FLM 36
Strenght 400MG
Pharmaceutical form Film-coated tablet
Package 36
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status OTC medicinal products
Active substance IBUPROFEN (IBUPROFENUM)
ATC group M01AE01
ATC group name IBUPROFEN

Marketing authorisation information

Registration Number 29/ 154/88-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. 2018
MA Holder Zentiva, k.s., 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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