Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Solid dosage forms aspirin

Many examples of the effects of tablet excipients on dmg decompositions are reported in the pharmaceutical literature. Chemical interaction between components in solid dosage forms may lead to increased decomposition. Replacement of the phenacetin in compound codeine and ARC tablets by paracetamol in NHS formulations in Australia in the 1960s (because of the undesirable side-effects of phenacetin), led to an unexpected decreased stability of the tablets. The cause was later attributed to a transacetylation reaction between aspirin and paracetamol and also a possible direct hydrolysis of the paracetamol (Scheme 4.15). [Pg.125]

Patel S, Perrin JH, Windheuser JJ (1972) GLC analysis of aspirin from solid dosage forms. J Pharm Sci 61 1794-1796... [Pg.72]

Galante, R.N. Visalli, A.J. Grim, W.M. Stabilized normal-phase high-performmce liquid chromatographic analysis of aspirin and salicylic acid in solid pharmaceutical dosage forms. J.Pharm.Sci., 1984, 73, 195-197... [Pg.131]

See other pages where Solid dosage forms aspirin is mentioned: [Pg.54]    [Pg.650]    [Pg.913]    [Pg.689]    [Pg.1653]    [Pg.3947]    [Pg.446]    [Pg.447]    [Pg.70]    [Pg.140]    [Pg.5]    [Pg.142]    [Pg.253]    [Pg.144]    [Pg.369]    [Pg.139]    [Pg.162]    [Pg.725]    [Pg.258]    [Pg.503]    [Pg.4697]    [Pg.71]   
See also in sourсe #XX -- [ Pg.4106 ]



SEARCH



Dosage solid

Solid dosage forms

Solid forms

© 2024 chempedia.info