A: The RF value of the principal spot observed in the chromatogram of the Test preparation obtained as directed in the Chromatographic purity test corresponds to that obtained from the Standard preparation.

B: The retention time of the major peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation, as obtained in the Assay.

Test preparation— Dilute Injection quantitatively with water, if necessary, to obtain a solution containing 25 mg of ranitidine per mL. [NOTE—Use Injection of lower concentration without dilution as directed under Procedure.]

Standard preparation— Dissolve USP Ranitidine Hydrochloride RS in water to obtain a solution having a known concentration of 560 µg per mL. Dilute portions of this Standard preparation quantitatively with water to obtain solutions having concentrations of 280 µg per mL (Diluted standard preparation A), 140 µg per mL (Diluted standard preparation B), 84 µg per mL (Diluted standard preparation C), 28 µg per mL (Diluted standard preparation D), and 14 µg per mL (Diluted standard preparation E), respectively.

Resolution preparation— Dissolve USP Ranitidine Related Compound A RS in methanol to obtain a solution having a known concentration of 1.27 mg per mL.

Procedure— Apply separately 10 µL of the Standard preparation, Diluted standard preparations A, B, C, D and E, and the required volume of the Test preparation, equivalent to 250 µg of ranitidine, to a suitable thin-layer chromatographic plate (see Chromatography 621) coated with a 0.25-mm layer of chromatographic silica gel mixture. In addition, apply separately a further loading of the same volume of the Test preparation to the same plate, and on top of this application, apply 10 µL of the Resolution preparation. Allow the spots to dry, and develop the chromatograms in a solvent system consisting of a mixture of ethyl acetate, isopropyl alcohol, ammonium hydroxide, and water (25:15:5:1) until the solvent front has moved not less than 15 cm from the origin. Remove the plate from the developing chamber, mark the solvent front, and allow to air-dry. Expose the plate to iodine vapors in a closed chamber until the chromatogram is fully revealed. Examine the plate and compare the intensities of any secondary spots observed in the chromatogram of the Test preparation with those of the principal spots in the chromatograms of the Standard preparation and Diluted standard preparations (A, B, C, D, and E): the system suitability requirements are met when there is complete resolution between the primary spots of the Test preparation, and the Resolution preparation and if a spot is observed in the chromatogram of Diluted standard preparation E. The major secondary spot is not greater in size or intensity than the principal spot produced by the Standard preparation (2.0%), and no other secondary spot is greater in size or intensity than the principal spot produced by Diluted standard preparation A (1.0%). The sum of the intensities of all secondary spots obtained from the Test preparation, corresponds to not more than 5.0%.

Mobile phase— Prepare a filtered and degassed mixture of methanol and 0.1 M aqueous ammonium acetate (85 : 15). Make adjustments if necessary (see System Suitability under Chromatography 621).

Standard preparation— Dissolve an accurately weighed quantity of USP Ranitidine Hydrochloride RS in Mobile phase to obtain a solution having a known concentration of about 0.112 mg (equivalent to 0.100 mg of ranitidine base) per mL.

System suitability solution— Dissolve accurately weighed quantities of USP Ranitidine Hydrochloride RS and USP Ranitidine Related Compound C RS in Mobile phase to obtain a solution having known concentrations of about 0.112 mg per mL and 0.01 mg per mL, respectively.

Assay preparation— Dilute an accurately measured volume of Injection, quantitatively and stepwise if necessary, with Mobile phase to obtain a solution having a concentration of 0.1 mg of ranitidine per mL.

Chromatographic system (see Chromatography 621)— The liquid chromatograph is equipped with a 322-nm detector and a 4.6-mm × 20- to 30-cm column that contains packing L1. The flow rate is about 2 mL per minute. Chromatograph the System suitability solution, and record the peak responses as directed for Procedure: the resolution, R, between ranitidine hydrochloride and N-[2-[[[5-[(dimethylamino)methyl]-2-furanyl]methyl]sulfinyl]ethyl]-N¢-methyl-2-nitro-1,1-ethenediamine (ranitidine related compound C) is not less than 1.5. Chromatograph the Standard preparation, and record the peak responses as directed for Procedure: the tailing factor for the ranitidine hydrochloride peak is not more than 2.0; the column efficiency determined from the ranitidine hydrochloride peak is not less than 700 theoretical plates; and the relative standard deviation for replicate injections is not more than 2%.

Procedure— Separately inject equal volumes (about 10 µL) of the Standard preparation and the Assay preparation into the chromatograph, record the chromatograms, and measure the area responses for the major peaks. Calculate the quantity, in mg, of C13H22N4O3S in the portion of Injection taken by the formula: in which 314.40 and 350.87 are the molecular weights of ranitidine and ranitidine hydrochloride, respectively; L is the labeled quantity of ranitidine in the Injection taken; D is the concentration, in mg per mL, of ranitidine in the Assay preparation on the basis of the labeled quantity and the extent of dilution; C is the concentration, in mg per mL, of USP Ranitidine Hydrochloride RS in the Standard preparation; and rU and rS are the peak area responses obtained from the Assay preparation and the Standard preparation, respectively.