FIELD: pharmacy. SUBSTANCE: invention relates to a solid pharmaceutical dosing form that provides the slow release of drug. The form is obtained by direct pressing cross-linked amylose of different cross-linking degree, α--amylase and a pharmaceutical agent. Cross-linked amylose ensures to provide the gradual drug release and α--amylase ensures to modulate time of release. Amount of α--amylase is 100 or less enzymatic units. EFFECT: improved quality and properties of the form. 5 cl, 5 dwg, 5 ex
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