Dicyclomine Hydrochloride Tablets
» Dicyclomine Hydrochloride Tablets contain not less than 93.0 percent and not more than 107.0 percent of the labeled amount of dicyclomine hydrochloride (C19H35NO2·HCl).
Packaging and storage— Preserve in well-closed containers.
Identification—
A: Transfer a portion of finely powdered Tablets, equivalent to about 100 mg of dicyclomine hydrochloride, to a separator containing 10 mL of water and 1 mL of hydrochloric acid. Proceed as directed in Identification test A under Dicyclomine Hydrochloride Capsules, beginning with “Extract the aqueous acid solution.”
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 711
Medium: 0.01 N hydrochloric acid; 500 mL.
Apparatus 2: 50 rpm.
Time: 45 minutes.
Mobile phase, 0.04 M Phosphate buffer, pH 7.5, Buffer–acetonitrile mixture, Test solution, and Chromatographic system— Proceed as directed for Dissolution under Dicyclomine Hydrochloride Capsules.
Standard solution— Prepare a solution in Medium having a known concentration of about 40 µg per mL of USP Dicyclomine Hydrochloride RS. Transfer 25.0 mL of this solution to a suitable flask, add 25.0 mL of the Buffer–acetonitrile mixture, and mix.
Procedure— Proceed as directed for Dissolution under Dicyclomine Hydrochloride Capsules.
Tolerances— Not less than 75% (Q) of the labeled amount of C19H35NO2·HCl is dissolved in 45 minutes.
Uniformity of dosage units 905: meet the requirements.
Assay—
0.02 M Phosphate buffer, pH 7.5, Mobile phase, Diluent, Standard preparation, and Chromatographic system— Prepare as directed in the Assay under Dicyclomine Hydrochloride Capsules.
Assay preparation— Transfer not fewer than 20 Tablets to a tared container, and determine the average Tablet weight. Grind the Tablets to a fine powder using a glass mortar and pestle. Transfer an accurately weighed portion of the powder, equivalent to about 20 mg of dicyclomine hydrochloride, to a 50-mL volumetric flask. Proceed as directed under Dicyclomine Hydrochloride Capsules beginning with “Add 2.0 mL of water.”
Procedure— Proceed as directed in the Assay under Dicyclomine Hydrochloride Capsules. Calculate the quantity, in mg, of dicyclomine hydrochloride (C19H35NO2·HCl) in the portion of Tablets taken by the formula:
50C(rU / rS)
in which C is the concentration, in mg per mL, of USP Dicyclomine Hydrochloride RS in the Standard preparation; and the other terms are as defined therein.
Auxiliary Information— Please check for your question in the FAQs before contacting USP.
Topic/Question Contact Expert Committee
Monograph Elena Gonikberg, Ph.D.
Senior Scientist
1-301-816-8251
(MDGRE05) Monograph Development-Gastrointestinal Renal and Endocrine
Reference Standards Lili Wang, Technical Services Scientist
1-301-816-8129
RSTech@usp.org
711 Margareth R.C. Marques, Ph.D.
Senior Scientist
1-301-816-8106
(BPC05) Biopharmaceutics05
USP32–NF27 Page 2130
Pharmacopeial Forum: Volume No. 30(3) Page 834
Chromatographic Column—
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.