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IBALGIN PLUS

400MG/100MG TBL FLM 10

SÚKL code 0228516
Name of the product IBALGIN PLUS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i IBALGIN PLUS
Supplement 400MG/100MG TBL FLM 10
Strenght 400MG/100MG
Pharmaceutical form Film-coated tablet
Package 10
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status OTC medicinal products
Active substance CAFFEINE (COFFEINUM)
IBUPROFEN (IBUPROFENUM)
ATC group M01AE51
ATC group name IBUPROFEN, KOMBINACE

Marketing authorisation information

Registration Number 07/ 106/18-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Concerned 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. 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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