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White to off-white, capsule shaped, uncoated tablets, debossed with '41' on one side and 'J' on the other side. Treatment should be initiated by or under the supervision of a physician with appropriate knowledge of indicated disorders see section 4. The recommended starting daily dose is mg. The total daily dose may be taken as a single dose in the morning or as two doses, one in the morning and at one noon, according to physician assessment of the patient and the patient's response. Doses of up to mg in one or two divided doses can be used in patients with insufficient response to the initial mg modafinil dose.

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Modafinil has emerged as the crown prince of smart drugs, that seductive group of pharmaceutical friends that promise enhanced memory, motivation, and an unrelenting ability to focus, all for hours at a time. In the absence of long-term data, the media, particularly the student media, has tended to be relaxed about potential side-effects. The Oxford Tab, for example, simply shrugs: Who cares? The novelist MJ Hyland, who suffers from multiple sclerosis, wrote a paean to the drug in the Guardian recently — understandably, for her, any potential side-effects are worth the risk given the benefits she's experienced. But should stressed students, tempted by a quick fix, be worried about what modafinil could be doing their brains in the long term?

The present invention provides pharmaceutical tablets comprising modafinil particles, processes for preparing such pharmaceutical tablets, and methods of treating a disease or disorder using the pharmaceutical tablet of the invention. The pharmaceutical tablet of the invention is prepared by a dry granulation method. In particular, the present invention relates to a pharmaceutical tablet comprising coarse modafinil particles, still exhibiting relatively rapid dissolution and processes for preparing such pharmaceutical tablets. The benzhydrylsulfinyl acetamide structure of modafinil makes it generally insoluble in water. One way to address the problem of insolubility is reducing the drug's particle size to increase the effective exposed surface area.

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