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Stability of Dosage Forms

The chemical and physical stability of pure drug substances has been described in Chapters 2 and 3, respectively. The stability of pharmaceutical dosage forms is described in this chapter. [Pg.151]


R. C. Schultz, Stability of Dosage Forms, FDA-Industry Interface Meeting, Washington, DC, Oct. 7, 1983 Stability Guidelines, Congressional Record, May 7, 1984. [Pg.191]

To a certain extent this is a sham for there are many of you who are doing analytical work related to animal toxicity experiments. Many of you supervise diet preparation technicians. Many of you either conduct on your own or supervise analytical technicians who conduct the basic work on stability of dosage forms, on homogeneity of dosage forms, on stability of test chemicals. [Pg.14]

Moisture adsorption by solid dosage forms can result not only in increased chemical drug degradation but also in changes in the functional stability of dosage forms. [Pg.174]


See other pages where Stability of Dosage Forms is mentioned: [Pg.593]    [Pg.373]    [Pg.649]    [Pg.654]    [Pg.923]    [Pg.387]    [Pg.38]    [Pg.139]    [Pg.151]    [Pg.152]    [Pg.154]    [Pg.156]    [Pg.158]    [Pg.159]    [Pg.162]    [Pg.164]    [Pg.166]    [Pg.168]    [Pg.170]    [Pg.172]    [Pg.174]    [Pg.175]    [Pg.176]    [Pg.178]    [Pg.180]    [Pg.182]    [Pg.184]    [Pg.186]    [Pg.466]    [Pg.231]   


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Stability, dosage form

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