CPC A61K 31/4709 (2013.01) [A61K 9/2013 (2013.01); A61K 9/2018 (2013.01); A61K 9/2027 (2013.01); A61K 9/2054 (2013.01); A61K 9/2095 (2013.01); A61K 9/4833 (2013.01); A61K 9/4858 (2013.01); A61K 9/4866 (2013.01)] | 17 Claims |
1. A pharmaceutical composition comprising an active ingredient (R, E)-N-(4-(3-chloro-4-(pyridin-2-ylmethoxy) phenylamino)-3-cyano-7-ethoxyquinolin-6-yl)-3-(1-methylpyrrolidinyl-2-yl)-acrylamide or a pharmacologically acceptable salt thereof, a disintegrant, a filler, an adhesive and a lubricant;
the pharmaceutical composition is obtained by a) mixing the active ingredient (R, E)-N-(4-(3-chloro-4-(pyridin-2-ylmethoxy) phenylamino)-3-cyano-7-ethoxyquinolin-6-yl)-3-(1-methylpyrrolidinyl-2-yl)-acrylamide or the pharmacologically acceptable salt thereof with the disintegrant, the filler, and the adhesive;
b) wet granulating by adding a wetting agent;
c) fluidized drying;
d) adding the lubricant and mixing; and
e) compressing into tablets or filling into capsules;
wherein the wetting agent is ethanol or ethanol and water, wherein the disintegrant is cross-linked polyvinyl pyrrolidone, and wherein the wet granulating is fluidized bed spray granulating.
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