IBALGIN PLUS
400MG/100MG TBL FLM 10
SÚKL code | 0228516 |
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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 |
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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 |