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ARCOXIA

90MG TBL FLM 14

SÚKL code 0098950
Name of the product ARCOXIA
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ARCOXIA
Supplement 90MG TBL FLM 14
Strenght 90MG
Pharmaceutical form Film-coated tablet
Package 14
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance ETORICOXIB (ETORICOXIBUM)
ATC group M01AH05
ATC group name ETORIKOXIB

Marketing authorisation information

Registration Number 29/ 077/03-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. 10. 2022
MA Holder Merck Sharp & Dohme B.V., Haarlem
MA Holder country NIZOZEMSKO
Actual MA holder N.V. Organon, Oss
Actual MA holder country NIZOZEMSKO

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