Process for obtaining pharmaceutical sustained releases

Claim 1

A process of preparing a dry, pharmaceutical delayed action composition suitable for oral administration in which at least one therapeutically active ingredient is dispersed in a vehicle or matrix of particulate talc, said talc being almost insoluble in the fluids of the digestive tract and the particles thereof being bound together by a binder consisting of a solid, water-insoluble, organosoluble, ethyl cellulose which comprises preparing a dry mixture by mixing in the dry powdered state the therapeutically active ingredient, the talc, and the binder, in the proportions of about 1 to 5 parts of talc for each part of active ingredient and about 16 and 59 parts of dry mixture for each part of binder, with the further proviso that there be present at least twice as much talc as ethyl cellulose, wetting the powder mixture with solvent in which the binder is soluble and in which the talc is insoluble in an amount just sufficient to insure granulation, and then granulating the resultant wetter powder mixture, drying the granules, incorporating therein as a tableting lubricant from about 2/3 to 2% of magnesium stearate, and tableting the resulting mixture.