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J Pharm Sci ; 64(2): 328-32, 1975 Feb.
Article in English | MEDLINE | ID: mdl-1127590

ABSTRACT

Incorporation of starch USP or a modified cornstarch within the granules of several drug formulations was investigated. In general, the formulation containing the modified starch exhibited improved processing characteristics as well as improved tablet properties. A comparison of a granulated and a direct compression formulation of the same ingradients indicated that granulation of an active ingredient is not necessarily detrimental to its (pharmaceutical) availability.


Subject(s)
Starch , Acetaminophen , Ascorbic Acid , Biopharmaceutics , Cellulose , Chlorothiazide , Dihydroxyphenylalanine , Excipients , Hardness Tests , Kinetics , Methyldopa , Pressure , Probenecid , Solubility , Starch/standards , Tablets/standards
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