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 or in the bottleafter 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 the packaging and medications you no longer need at the SIGRE collection pointof the pharmacy. If in doubt, ask your pharmacist how to dispose of the packaging and medications you no longer need. By doing so, you will help protect the environment.
Composition ofEtoricoxib TecniGen
The active ingredient is etoricoxib. Each film-coated tablet contains 30 mg, 60 mg, 90 mg or 120 mg of etoricoxib.
The other components (excipients) are:
Etoricoxib TecniGen 30 mg, 60 mg, 120 mg film-coated tablets:
Core: microcrystalline cellulose, anhydrous calcium hydrogen phosphate, croscarmellose sodium, magnesium stearate.
Coating: lactose monohydrate, hypromellose 2910/15 cp, titanium dioxide (E171), triacetin, indigo carmine FDC Blue No. 2 (E132), yellow iron oxide (E172).
Etoricoxib TecniGen 90 mg film-coated tablets:
Core: microcrystalline cellulose, anhydrous calcium hydrogen phosphate, croscarmellose sodium, magnesium stearate.
Coating: lactose monohydrate, hypromellose 2910/15 cp, hypromellose 2910/50 cp, titanium dioxide (E171), triacetin.
Appearance ofEtoricoxib TecniGenand contents of the package
Etoricoxib TecniGen 30 mg film-coated tablets:
Round, green film-coated tablets.
Etoricoxib TecniGen 60 mg film-coated tablets:
Oblong, green film-coated tablets.
Etoricoxib TecniGen 90 mg film-coated tablets:
Round, white film-coated tablets.
Etoricoxib TecniGen 120 mg film-coated tablets:
Round, green film-coated tablets.
Package sizes:
Etoricoxib TecniGen 30 mg, 60 mg, 90 mg film-coated tablets:available in blister packs containing 28 tablets.
Etoricoxib TecniGen 120 mg film-coated tablets:available in blister packs containing 7 tablets.
Marketing authorization holder
Tecnimede España Industria Farmacéutica, S.A.
Avda. de Bruselas, 13, 3º D. Edificio América. Polígono Arroyo de la Vega,
28108 Alcobendas (Madrid). SPAIN
Responsible for manufacturing
Atlantic Pharma – Produções Farmacêuticas, S.A.
Rua da Tapada Grande, nº2, Abrunheira
2710-089 Sintra
Portugal
Last revision date of this leaflet: March 2018
The detailed and updated information on this medicine is available on the website of the Spanish Agency for Medicines and Medical Devices (AEMPS) http://www.aemps.gob.es
Have questions about this medication or your symptoms? Connect with a licensed doctor for guidance and personalized care.