COMBOGESIC

500MG/150MG TBL FLM 16

SÚKL code 0223547
Name of the product COMBOGESIC 500 MG/150 MG POTAHOVANÉ TABLETY
_MA_MEDICATION_DETAIL_INFO_MED_NAME i COMBOGESIC
Supplement 500MG/150MG TBL FLM 16
Strenght 500MG/150MG
Pharmaceutical form Film-coated tablet
Package 16
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance PARACETAMOL (PARACETAMOLUM)
IBUPROFEN (IBUPROFENUM)
ATC group N02BE51
ATC group name PARACETAMOL, KOMBINACE KROMĚ PSYCHOLEPTIK

Marketing authorisation information

Registration Number 07/ 073/15-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. 01. 2019
MA Holder Vale Pharmaceuticals Limited, Clonmel
MA Holder country IRSKO
Actual MA holder Amicus Pharma Kft., Budapešť
Actual MA holder country MAĎARSKO

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