The aim of this study was to prepare fast-dissolving tablets of meloxicam after its complexation with β-cyclodextrin (β-CD) and to investigate the effect of using different superdisintegrants on the disintegration and release of meloxicam from the tablets. A complex of meloxicam with β-CD was prepared by spray drying and then compressed in the form of tablets utilizing the direct compression technique. Three superdisintegrants were employed at various levels - sodium starch glycolate, croscarmellose sodium, and crospovidone. Co-spray dried micro-crystalline cellulose and mannitol (Avicel HFE-102) were used as diluents in the tablets. Prior to compression, the pre-compression parameters showed satisfactory flow properties. Post-compression parameters showed that all tablet formulations had acceptable mechanical properties. Wetting and disintegration times were prolonged by increasing the level of sodium starch glycolate in the tablets. This was attributed to the formation of a viscous gel layer around the tablets by sodium starch glycolate whereas this effect was not observed with croscarmellose sodium and crospovidone. Dissolution studies showed fast release of meloxicam except in tablets containing a high level of sodium starch glycolate. Complexation of meloxicam with β-CD significantly improved the solubility of the drug and improved the mechanical properties of tablets produced by direct compression. Cilj rada bio je priprava lako topljivih tableta kompleksa meloksikama s β-ciklodekstrinom (β-CD) te ispitati utjecaj različitih superdezintegratora na raspadljivost tableta i oslobađanje meloksikama. Kompleks meloksikama s β-CD pripravljen je metodom sušenja sprejem, a komprimiran je u tablete metodom izravne kompresije. U pripravi tableta korištene su tri različite količine triju superdezintegratora: natrijev škrobni glikolat, natrijeva sol kroskarmeloze i krospovidon, dok su mikrokristalinična celuloza i manitol (Avicel HFE-102) upotrijebljeni kao punila. Predkompresijski parametri ukazivali su na zadovoljavajuću tečnost. Postkompresijski parametri pokazali su da sve tablete imaju prihvatljiva mehanička svojstva. Vlaženje i vrijeme raspadanja bilo je produljeno kada se povećao udio natrijevog škrobnog glikolata u tabletama. To je pripisano stvaranju viskoznog sloja gela oko tableta, što nije primijećeno u pripravi tableta s natrijevom soli kroskarmeloze i krospovidonom. Oslobađanje meloksikama bilo je brzo iz svih tableta, osim iz tableta s visokim udjelom natrijeve soli škrobnog glikolata. Kompleksiranje meloksikama s β-CD značajno je povećalo topljivost lijeka i poboljšalo mehanička svojstva tableta.