Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date that appears on the packaging after CAD. The expiration date is the last day of the month indicated.
This medication does not require special storage conditions.
Medications should not be disposed of through drains or in the trash. Dispose of packaging and medications you no longer need at the SIGRE collection point at the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition of Etoricoxib Combix
Core of the tablet:sodium laurilsulfate, microcrystalline cellulose, hydroxypropylcellulose, anhydrous calcium hydrogen phosphate, croscarmellose sodium, anhydrous colloidal silica, magnesium stearate.
Coating of the tablet:monohydrate lactose, triacetin, hypromellose, and titanium dioxide (E171). The 30 mg, 60 mg, and 120 mg tablets also contain indigotin (Laca índigo carmín) (E132) and yellow iron oxide (E172).
Appearance of the product and contents of the package
Etoricoxib Combix tablets are available in 4 doses:
Etoricoxib Combix 30 mg film-coated tablets: presented in the form of smooth, film-coated, biconvex, round tablets, both sides greenish to bluish green.
Etoricoxib Combix 60 mg film-coated tablets: presented in the form of film-coated tablets with '60' engraved on one side and smooth on the other, biconvex, round, green.
Etoricoxib Combix 90 mg film-coated tablets: presented in the form of smooth, film-coated, biconvex, round tablets, both sides white to off-white.
Etoricoxib Combix 120 mg film-coated tablets: presented in the form of film-coated tablets with '120' engraved on one side and smooth on the other, biconvex, round, green.
Package sizes:
Etoricoxib Combix 30 mg, 60 mg, and 90 mg: 28 film-coated tablets.
Etoricoxib Combix 120 mg: 7 film-coated tablets.
Marketing Authorization Holder
Combix, S.L.U.
C/ Badajoz 2, Edificio 2
28223 Pozuelo de Alarcón (Madrid)
Spain
Responsible for manufacturing
Zydus France
ZAC Les Hautes Patures
Parc d'activités des Peupliers
25 Rue des Peupliers
92000 Nanterre
France
or
Centre Spécialités Pharmaceutiques
ZAC des Suzots
35 rue de la Chapelle
63450 Saint Amant Tallende
France
Last review date of this leaflet: April 2017
Detailed and updated information on this medication is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS)http://www.aemps.gob.es/
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