Two simple and sensitive methods for the determination of indapamide in pur
e and in dosage forms are developed. These methods are based on the oxidati
on of indapamide with iron(II) in acidic medium. The liberated iron(II) rea
cts with 1,10-phenanthroline (Method A) and the ferroin complex is colorime
trically measured at lambda (max) 509 nm against reagent blank. Method B is
based on the reduction of Fe(III) by the drug. Iron(II) forms a colored co
mplex (lambda (max) 522 nm) with 2,2'-bipyridyl. Optimization of the experi
mental conditions is described. Beer's law is obeyed in the concentration r
ange 1.0-12 mug ml(-1) and 4.0-18 mug ml(-1) for A and B, respectively. The
apparent molar absorptivity and Sandell sensitivity for method A is 3 x 10
(4) L mol(-1) cm(-1) and 0.0188 mug cm(-2), while for method B is 2.3 x 10(
4) L mol(-1) cm(-1) and 0.0159 mug cm(-2). The detection and quantification
limits are calculated. The developed methods are applied successfully for
the determination of indapamide in pure and in tablet form without interfer
ence from common excepients.