Fexofenadine Hydrochloride Tablets
» Fexofenadine Hydrochloride Tablets contain not less than 95.0 percent and not more than 105.0 percent of the labeled amount of fexofenadine hydrochloride (C32H39NO4·HCl).
Packaging and storage—
Preserve in well-closed containers, and store at controlled room temperature.
Labeling—
When more than one Dissolution test is given, the labeling states the test used only if Test 1 is not used.
USP Reference standards
![]() ![]() USP Fexofenadine Hydrochloride RS. USP Fexofenadine Related Compound A RS.
Identification—
A:
Infrared Absorption
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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.
Dissolution
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Test 1—
Medium:
0.001 N hydrochloric acid; 900 mL, deaerated.
Apparatus 2:
50 rpm.
Times:
10 and 30 minutes.
Determine the percentages of the labeled amount of fexofenadine hydrochloride (C32H39NO4·HCl) dissolved by using the following method.
Buffer solution—
Dissolve 1.0 g of monobasic sodium phosphate, 0.5 g of sodium perchlorate, and 0.3 mL of concentrated phosphoric acid in 300 mL of water, and mix.
Mobile phase—
Prepare a filtered and degassed mixture of acetonitrile and Buffer solution (7:3). Make adjustments if necessary (see System Suitability under Chromatography
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Standard solution—
[note—A small amount of methanol, not exceeding 0.5% of the total volume, can be used to dissolve fexofenadine hydrochloride.] Dissolve an accurately weighed quantity of USP Fexofenadine Hydrochloride RS in Medium to obtain a solution having a known concentration similar to that expected for the solution under test.
Resolution solution—
[note—A small amount of acetic acid, not exceeding 5% of the total volume, can be used to dissolve fexofenadine hydrochloride related compound A.] Dissolve an accurately weighed quantity of USP Fexofenadine Related Compound A RS in water to obtain a solution having a known concentration of about 0.44 mg per mL. Transfer 1.0 mL of this solution into a vial, add 40 mL of the Standard solution, and mix.
Test solution—
Use portions of the solution under test passed through a 0.45-µm glass fiber filter.
Chromatographic system (see Chromatography
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Procedure—
Separately inject equal volumes (approximately 2 to 3 µg column load of fexofenadine hydrochloride) of the Standard solution and the Test solution into the chromatograph, record the chromatograms, and measure the responses for the fexofenadine peaks. Calculate the quantity, in mg, of fexofenadine hydrochloride (C32H39NO4·HCl) dissolved in the Medium by the formula:
CD(rU / rS)
in which C is the concentration, in mg per mL, of USP Fexofenadine Hydrochloride RS in the Standard solution; D is the dilution factor used in preparing the Test solution; and rU and rS are the fexofenadine peak areas obtained from the Test solution and the Standard solution, respectively.
Tolerances—
Not less than 60% (Q) of the labeled amount of C32H39NO4·HCl is dissolved in 10 minutes; and not less than 80% (Q) of the labeled amount of C32H39NO4·HCl is dissolved in 30 minutes.
test 2—
If the product complies with this test, the labeling indicates that the product meets USP Dissolution Test 2.
Medium:
0.001 N hydrochloric acid; 900 mL.
Apparatus 2:
50 rpm, use paddles and shafts coated with Teflon.
Time:
30 minutes.
Determine the percentage of the labeled amount of fexofenadine hydrochloride (C32H39NO4·HCl) dissolved by employing the following method.
Buffer solution—
Dissolve 7.0 g of ammonium acetate in 1000 mL of water. Adjust with glacial acetic acid to a pH of 4.0 ± 0.05.
Mobile phase—
Prepare a filtered and degassed mixture of Buffer solution and acetonitrile (3:2). Make adjustments if necessary (see System Suitability under Chromatography
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Standard solution 1—
Transfer about 20 mg, accurately weighed, of USP Fexofenadine Hydrochloride RS to a 100-mL volumetric flask. Add 3.0 mL of methanol, and mix. Dilute with Medium to volume, and mix.
Standard solution 2—
Transfer 15.0 mL of Standard solution 1 to a 50-mL volumetric flask, dilute with Medium to volume, and mix.
Standard solution 3—
Transfer 7.5 mL of Standard solution 1 to a 50-mL volumetric flask, dilute with Medium to volume, and mix.
Test solution—
Use portions of the solution under test passed through a suitable 0.45-µm filter.
Chromatographic system (see Chromatography
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Procedure—
Separately inject equal volumes (30 µL for Standard solution 2 and 3, and 10 µL for Standard solution 1) of the appropriate Standard solution and the Test solution into the chromatograph, record the chromatograms, and measure the responses for the fexofenadine peak. Calculate the percentage of fexofenadine hydrochloride (C32H39NO4·HCl) dissolved by the formula:
in which rU and rS are the peak responses for the Standard solution and the Test solution, respectively; CS is the concentration, in mg per mL, of the appropriate Standard solution; 900 is the volume, in mL, of Medium; 100 is the conversion factor to percentage; and L is the tablet label claim, in mg.
Tolerances—
Not less than 75% (Q) of the labeled amount of C32H39NO4·HCl is dissolved in 30 minutes.
Uniformity of dosage units
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Related compounds—
Diluent and Mobile phase—
Prepare as directed in the Assay.
Sensitivity solution—
Dilute 4.0 mL of the Standard stock preparation, prepared as directed in the Assay, with Mobile phase to 100 mL. Dilute 6.0 mL of this solution with Mobile phase to 100 mL.
Related compound solution—
Dissolve an accurately weighed quantity of USP Fexofenadine Related Compound A RS in Diluent, and dilute quantitatively, and stepwise if necessary, with Diluent to obtain a solution having a known concentration of about 0.05 mg per mL.
Standard stock solution—
Use the Standard stock preparation, prepared as directed in the Assay.
Standard solution—
Dilute accurate volumes of the Related compound solution and the Standard stock solution with Mobile phase to obtain a solution having known concentrations of about 0.015 and 0.0045 mg per mL of fexofenadine hydrochloride and fexofenadine related compound A, respectively.
Test stock solution—
Use the Assay stock preparation.
Test solution—
Use the Assay preparation.
Chromatographic system (see Chromatography
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Procedure—
Separately inject equal volumes (about 20 µL) of the Standard solution, the Test stock solution, and the Test solution into the chromatograph, record the chromatograms, and measure the peak responses. Calculate the percentage of fexofenadine related compound A in the portion of Tablets taken by the formula:
100CD(ri / rS)/NL
in which C is the concentration, in mg per mL, of fexofenadine related compound A in the Standard solution; D is the dilution factor for the preparation of the Test stock solution, in mL; ri and rS are the peak area responses of fexofenadine related compound A in the Test stock solution and the Standard solution, respectively; N is the number of Tablets used to prepare the Test stock solution; and L is the label claim, in mg per Tablet, of fexofenadine hydrochloride. Calculate the percentage of the decarboxylated degradant [(+)-4-[1-hydroxy-4-[4-(hydroxydiphenylmethyl)-1-piperidinyl]-butyl]-isopropylbenzene; the relative retention time is 6.7] in the portion of Tablets taken by the formula:
100CD(ri / rS)/NLF
in which C is the concentration, in mg per mL, of USP Fexofenadine Hydrochloride RS in the Standard solution; D is the dilution factor for the preparation of the Test stock solution in mL; ri is the peak area response of the decarboxylated degradant in the Test stock solution; rS is the peak area response of fexofenadine in the Standard solution; N is the number of Tablets used to prepare the Test stock solution; L is the label claim, in mg per Tablet, of fexofenadine hydrochloride; and F is the relative response factor (F is 1.1) for the decarboxylated degradant (F is 1.0 for all other known and unknown impurities). Calculate the percentage of any other impurities in the portion of Tablets taken by the formula:
100ri / (DrS + rT)
in which ri is the individual peak area response for an individual unknown impurity in the Test stock solution; D is the dilution factor, in mL, of the Test solution; rS is the peak area response for fexofenadine in the Test solution; and rT is the sum of the peak area responses of all unknown impurities in the Test stock solution: disregard any peak below 0.05%; not more than 0.4% of fexofenadine related compound A is found; not more than 0.15% of the decarboxylated degradant is found; not more than 0.2% of any individual other impurity is found; and not more than 0.5% of total impurities is found.
Assay—
Acid solution—
Dilute 17 mL of glacial acetic acid with water to 1 L, and mix. Dilute 100 mL of this solution with water to 1 L.
Buffer solution—
Dilute 15 mL of a solution containing a mixture of acetonitrile and triethylamine (1:1) with Acid solution to 1 L. Adjust with phosphoric acid to a pH of 5.25.
Diluent—
Prepare a mixture of acetonitrile and Acid solution (75:25).
Mobile phase—
Prepare a filtered and degassed mixture of Buffer solution and acetonitrile (64:36). Make adjustments if necessary (see System Suitability under Chromatography
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Standard stock preparation—
Dissolve an accurately weighed quantity of USP Fexofenadine Hydrochloride RS in Diluent, and dilute quantitatively, and stepwise if necessary, with Diluent to obtain a solution having a known concentration of about 0.25 mg per mL.
Standard preparation—
Dilute an accurate volume of the Standard stock preparation with Mobile phase to obtain a solution having a known concentration of about 0.015 mg per mL.
Assay stock preparation—
Transfer a sufficient number of whole Tablets (not fewer than 10) to a suitable volumetric flask, add Acid solution (equivalent to about 20% of the total flask volume), and shake by mechanical means at a high speed for about 30 minutes or until the Tablets are fully disintegrated and finely dispersed. Add acetonitrile (equivalent to about 80% of the total flask volume), and shake by mechanical means for 60 minutes. Dilute with Diluent to volume, and mix. Pass a portion of this solution through a polytetrafluorethylene filter having a 0.45-µm or finer porosity, and use the filtrate. Dilute quantitatively, and stepwise if necessary, with Diluent to obtain a solution containing about 1.2 mg of fexofenadine hydrochloride per mL.
Assay preparation—
Dilute an aliquot of the Assay stock preparation quantitatively, and stepwise if necessary, with Mobile phase to obtain a solution containing about 0.018 mg of fexofenadine hydrochloride per mL.
Chromatographic system (see Chromatography
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Procedure—
Separately inject equal volumes (about 20 µL) of the Standard preparation and the Assay preparation into the chromatograph, record the chromatograms, and measure the responses for the fexofenadine peaks. Calculate the quantity, in mg per Tablet, of fexofenadine hydrochloride (C32H39NO4·HCl) in the portion of Tablets taken by the formula:
CD(rU / rS)/N
in which C is the concentration, in mg per mL, of USP Fexofenadine Hydrochloride RS in the Standard preparation; D is the dilution factor used for the Assay preparation; rU and rS are the peak responses obtained from the Assay preparation and the Standard preparation, respectively; and N is the number of Tablets used in the Assay preparation.
Auxiliary Information—
Please check for your question in the FAQs before contacting USP.
Chromatographic Column—
USP32–NF27 Page 2372
Pharmacopeial Forum: Volume No. 34(4) Page 931
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.
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