Procedure for content uniformity
Transfer 1 Tablet to a 50-mL volumetric flask. Add 20 mL of 0.5 N sulfuric acid and 10 mL of water, shake until the Tablet is disintegrated, and allow to stand for 16 hours. Dilute with water to volume, and filter, discarding the first few mL of the filtrate. Dilute a portion of the subsequent filtrate quantitatively and stepwise, if necessary, with 0.2 N sulfuric acid to obtain a solution containing approximately 120 µg of codeine sulfate (trihydrate) per mL. Concomitantly determine the absorbances of this solution and a Standard solution of
USP Codeine Sulfate RS in the same medium having a known concentration of about 110 µg per mL, in 1-cm cells, at the wavelength of maximum absorbance at about 284 nm, with a suitable spectrophotometer, using 0.2 N sulfuric acid as the blank. Calculate the quantity, in mg, of (C
18H
21NO
3)
2·H
2SO
4·3H
2O in the Tablet taken by the formula:
(750.87 / 696.82)(TC / D)(AU / AS),
in which 750.87 and 696.82 are the molecular weights of codeine sulfate trihydrate and anhydrous codeine sulfate, respectively;
T is the labeled quantity, in mg, of codeine sulfate in the Tablet;
C is the concentration, in µg per mL, of
USP Codeine Sulfate RS in the Standard solution;
D is the concentration, in µg per mL, of codeine sulfate in the test solution, based upon the labeled quantity per Tablet and the extent of dilution; and
AU and
AS are the absorbances of the test solution and the Standard solution, respectively.