FIELD: pharmacy. SUBSTANCE: composition comprises cisaprid-(L)-tartrate, pharmaceutically acceptable components, for example, carriers and excipients and from 15% to 35% of a mixture of hydroxypropylmethylcellulose with other cellulose derivative taken among the group including hydroxypropylcellulose, ethylcellulose, hydroxyethylcellulose, hydroxyethylmethyl-cellulose and methylcellulose of the composition mass. The mass ratio of hydroxypropylmethylcellulose and indicated cellulose derivative is from 0.33 to 3.0. The composition is prepared by mixing the indicated components. Cisaprid oral composition is used for treatment of gastrokinetic disorders and provides the release of an active component at the rate from the zero the first-order value. The indicated "pattern" of cisaprid release provides the rapid relief to patient and excludes the overdosing possibility at the following administration of the composition. EFFECT: improved properties and enhanced effectiveness of the composition. 6 cl, 4 ex
             
         
            
              
                | Title | Year | Author | Number | 
							
              
                | PARACETAMOL AND DOMPERIDONE TABLET WITH FILM COATING | 1995 |  | RU2153337C2 | 
							
              
                | COMPOSITIONS CONTAINING FINELY GROUND NEBIVOLOL | 1995 | 
										Egen JansGuido Frantsiskus SmansPol' Mari Viktor Gilis | RU2137473C1 | 
							
              
                | GRANULE, A METHOD OF ITS PREPARING AND A PHARMACEUTICAL COMPOSITION | 1993 | 
										Pol' Mari Viktor ZhiliValentin Floran Viktor De KondRozhe Petrjus Zherebern Vandekrjuj | RU2125445C1 | 
							
              
                | SABELUZOL AQUEOUS SUSPENSION FOR ORAL USE AND METHOD OF ITS PREPARING | 1995 | 
										Mark Karel Jozef FransuaKristin Frida Ogjusta Agemans | RU2141821C1 | 
							
              
                | DRUG COMPOSITIONS CONTAINING CONTROLLED RELEASE HYPROMELLOSE MATRIXES | 2006 | 
										Radzhabi-Siakhboomi AliFedzheli Kurt AlanJoung KaraRedzhe Pankadzh | RU2414241C2 | 
							
              
                | N-[[1-[4-(FLUOROPHENOXY)BUTYL]-4-PIPERIDINYL]-N-METHYLAMINO]-2-BENZTHIAZOLES OR THEIR PHARMACEUTICALLY ACCEPTABLE ACID SALTS, A METHOD OF SYNTHESIS, AN ANTIARRHYTHMIC COMPOSITION OF THE THIRD-CLASS AND A METHOD OF ITS PREPARING | 1994 | 
										Jozef Jan Piter KhejkantsMarsel' Jan Marija BorgersDoris Vil'Khel'M | RU2122546C1 | 
							
              
                | IMIDAZOAZEPINE DERIVATIVE, PHARMACEUTICAL COMPOSITION, METHOD OF ITS PREPARING, METHOD OF SYNTHESIS OF IMIDAZOAZEPINE DERIVATIVE | 1994 | 
										Frans Ehduard ZhansensJozef Ehlizabet Lehnarts | RU2133249C1 | 
							
              
                | PHARMACEUTICAL MULTILAYERED TABLET FOR CONTROLLED RELEASED OF ACTIVE COMPONENTS WITH SOLUBILITY, HIGHLY DEPENDING ON pH | 2005 | 
										Brjuehl' Zhan-LjukKjuin AlenRozhe Benedikt | RU2377976C2 | 
							
              
                | ESTER DERIVATIVES OF 9-HYDROXY-PYRIDO[1,2-A]PYRIMIDINE-4-ONE, A METHOD OF THEIR SYNTHESIS, A COMPOSITION SHOWING ANTIPSYCHOTIC ACTIVITY AND A METHOD OF ITS PREPARING | 1994 | 
										Jan VandenberkLjudo Ehdmon Zhozefin Kenni | RU2126406C1 | 
							
              
                | 4-(2-BEBZOTHIAZOLYL) METHYLAMINO ALPHA- (3,4- DIFLUOROPHENOXY) METHYL-1-PHARMACEUTICALLY ACID ADDITION SALT THEREOF, METHOD OF PREPARATION THEREOF, AND EFFECT ON BRAIN TISSUE | 1992 | 
										Rajmon Antuan Stokbroekks[Be]Zhil'Ber Artjur Zhjul' Grovel[Be] | RU2094434C1 |