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txalex

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Summary of the Invention
[0007] One general aspect, relates to a tablet of a clopidogrel salt comprising a therapeutically effective amount of a
clopidogrel salt; lactose; stearic acid; and one or more of other pharmaceutically acceptable excipients; wherein clopidogrel
salt is hydrobromide or hydrochloride.
[0008] Another aspect, relates to a tablet of a clopidogrel salt comprising a therapeutically effective amount of a
clopidogrel salt; lactose and microcrystalline cellulose; stearic acid; and one or more of other pharmaceutically acceptable
excipients wherein clopidogrel salt is hydrobromide or hydrochloride.
[0009] Yet another aspect, relates to a tablet of a clopidogrel salt comprising a therapeutically effective amount of a
clopidogrel salt; lactose; stearic acid and hydrogenated castor oil; and one or more of other pharmaceutically acceptable
excipients; wherein clopidogrel salt is hydrobromide or hydrochloride.
[0010] Another aspect, relates to a tablet of a clopidogrel salt comprising a therapeutically effective amount of a
clopidogrel salt; lactose and microcrystalline cellulose; stearic acid and hydrogenated castor oil; and one or more of
other pharmaceutically acceptable excipients; wherein clopidogrel salt is hydrobromide or hydrochloride.
[0011] Another aspect, relates to a tablet of a clopidogrel salt comprising a therapeutically effective amount of a
clopidogrel salt, prepared by process comprising the steps of
(a) blending the clopidogrel salt with the one or more of the diluents and other pharmaceutically acceptable excipients;
(b) mixing one or more of the lubricants with the blend of step (a); and
(c) compressing the final blend of step (b) into tablet;
wherein the clopidogrel salt is hydrobromide or hydrochloride.
[0012] A further aspect, relates to a tablet of a clopidogrel salt comprising a therapeutically effective amount of a
clopidogrel salt, prepared by process comprising the steps of
(a) blending the clopidogrel salt with lactose and other pharmaceutically acceptable excipients;
(b) mixing stearic acid with the blend of step (a); and
(c) compressing the final blend of step (b) into tablet;
wherein the clopidogrel salt is hydrobromide or hydrochloride.
[0013] Another aspect, relates to a tablet of a clopidogrel salt comprising a therapeutically effective amount of a
clopidogrel salt, prepared by process comprising the steps of
(a) blending the clopidogrel salt with lactose and microcrystalline cellulose and optionally other pharmaceutically
acceptable excipients;
(b) mixing stearic acid with the blend of step (a); and
(c) compressing the final blend of step (b) into tablet;
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