Procedure for content uniformity
Transfer 1 Tablet, previously crushed or finely powdered, to a 50-mL volumetric flask, add 25 mL of water, and shake to dissolve. Dilute with water to volume, and filter, if necessary, discarding the first 20 mL of the filtrate. Transfer an aliquot of the filtrate, equivalent to about 6 mg of codeine phosphate, to a 50-mL volumetric flask containing 2 mL of 3 N hydrochloric acid, and dilute with water to volume. Dissolve an accurately weighed quantity of
USP Codeine Phosphate RS in 0.1 N hydrochloric acid, and dilute quantitatively and stepwise with the same solvent to obtain a Standard solution having a known concentration of about 120 µg per mL. Concomitantly determine the absorbances of both solutions in 1-cm cells at the wavelength of maximum absorbance at about 284 nm, with a suitable spectrophotometer, using water as the blank. Calculate the quantity, in mg, of C
18H
21NO
3·H
3PO
4·½H
2O in the Tablet taken by the formula:
2.5(C / V)(AU / AS)(406.37 / 397.37),
in which
C is the concentration, in µg per mL, of
USP Codeine Phosphate RS in the Standard solution;
V is the volume, in mL, of the aliquot taken of the solution of the Tablet;
AU and
AS are the absorbances of the solution from the Tablet and the Standard solution, respectively; and 406.37 and 397.37 are the molecular weights of codeine phosphate hemihydrate and anhydrous codeine phosphate, respectively.