Keep this medication out of the sight and reach of children.
Do not use this medication after the expiration date indicated on the packaging. The expiration date refers to the last day of that month.
Store below 30°C.
Medicines should not be disposed of through drains or in the trash. Dispose of packaging and unused medications at the SIGRE collection pointat the pharmacy. If in doubt, ask your pharmacist how to dispose of packaging and unused medications. By doing so, you will help protect the environment.
Composition ofEtoricoxib Viso Pharmaceutical
Core of the tablet: Dicalcium phosphate anhydrous (Calipharm A), microcrystalline cellulose (Avicel PH 101), croscarmellose sodium (Ac-di-sol), magnesium stearate, microcrystalline cellulose (Avicel PH 200 LM)
Coating of the tablet:
For 30 mg, 60 mg, and 120 mg
Hydroxypropyl methylcellulose, titanium dioxide (E171), macrogol, aluminium lake of carmine (E132), iron oxide yellow (E172), isopropyl alcohol, methylene chloride (dichloromethane)
For 90 mg
Hydroxypropyl methylcellulose, titanium dioxide (E171), macrogol, isopropyl alcohol, methylene chloride (dichloromethane)
Appearance of the product and content of the package
Etoricoxib Viso Pharmaceutical tablets are available in four concentrations:
30 mg tablets: green-blue, biconvex, round film-coated tablets with the mark “11” on one side and “G” on the other, approximately 6 mm in diameter.
60 mg tablets: dark green, biconvex, round film-coated tablets with the mark “76” on one side and “G” on the other, approximately 8 mm in diameter.
90 mg tablets: white, biconvex, round film-coated tablets with the mark “757” on one side and “G” on the other, approximately 9 mm in diameter.
120 mg tablets: light green, biconvex, round film-coated tablets with the mark “758” on one side and “G” on the other, approximately 10.5 mm in diameter.
30 mg tablets: package sizes of 5, 28, 30, 90, 98 tablets in blister packs.
60 mg and 90 mg tablets: package sizes of 7, 14, 20, 28, 30, 50, 90, 100 tablets in blister packs.
120 mg tablets: package sizes of 2, 5, 7, 14, 20, 28, 30, 90 tablets in blister packs.
Only some package sizes may be marketed.
Holder of the marketing authorization and responsible for manufacturing
Holder of the marketing authorization
Glenmark Arzneimittel GmbH
Industriestr. 31,
82194 Gröbenzell,
Germany
Responsible for manufacturing
Pharmadox Healthcare Ltd.
KW20A Kordin Industrial Park,
Paola PLA3000,
Malta
Glenmark Pharmaceuticals s.r.o
Fibichova, 143
56617 Vysoke Myto, Czech Republic
You can request more information about this medication by contacting the local representative of the holder of the marketing authorization:
Viso Farmacéutica, S.L.U.
c/ Retama 7, 7th Floor,
28045 Madrid,
Spain
This medication is authorized in the EEA member states with the following names:
Country | Name |
Netherlands (EMR) | Etoricoxib Glenmark 30 mg filmomhulde tabletten Etoricoxib Glenmark 60 mg filmomhulde tabletten Etoricoxib Glenmark 90 mg filmomhulde tabletten Etoricoxib Glenmark 120 mg filmomhulde tabletten |
Germany | Etoricoxib Glenmark 30 mg Filmtabletten Etoricoxib Glenmark 60 mg Filmtabletten Etoricoxib Glenmark 90 mg Filmtabletten Etoricoxib Glenmark 120 mg Filmtabletten |
Greece | Etoricoxib Pharmazac 30 mg επικαλυμμ?ναμελεπτ?υμ?νιο δισκ?α Etoricoxib Pharmazac 60 mg επικαλυμμ?ναμελεπτ?υμ?νιο δισκ?α Etoricoxib Pharmazac 90 mg επικαλυμμ?ναμελεπτ?υμ?νιο δισκ?α Etoricoxib Pharmazac 120 mg επικαλυμμ?ναμελεπτ?υμ?νιο δισκ?α |
Spain | Etoricoxib Viso Farmacéutica 30 mg film-coated tablets EFG Etoricoxib Viso Farmacéutica 60 mg film-coated tablets EFG Etoricoxib Viso Farmacéutica 90 mg film-coated tablets EFG Etoricoxib Viso Farmacéutica 120 mg film-coated tablets EFG |
Last review date of the leaflet: November 2016
Detailed information about 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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