OMEBOIX

20MG CPS ETD 100 I

SÚKL code 0236122
Name of the product OMEBOIX
_MA_MEDICATION_DETAIL_INFO_MED_NAME i OMEBOIX
Supplement 20MG CPS ETD 100 I
Strenght 20MG
Pharmaceutical form Gastro-resistant capsule, hard
Package 100 I
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance OMEPRAZOLE (OMEPRAZOLUM)
ATC group A02BC01
ATC group name OMEPRAZOL

Marketing authorisation information

Registration Number 09/ 330/18-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. 08. 2020
MA Holder Esteve Pharmaceuticals S.A., Barcelona
MA Holder country ŠPANĚLSKO
Actual MA holder TOWA Pharmaceutical Europe, S.L., Martorelles (Barcelona)
Actual MA holder country ŠPANĚLSKO

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