U.S. PHARMACOPEIA

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Neomycin Sulfate and Hydrocortisone Otic Suspension
» Neomycin Sulfate and Hydrocortisone Otic Suspension is a sterile suspension containing not less than 90.0 percent and not more than 130.0 percent of the labeled amount of neomycin, and not less than 90.0 percent and not more than 110.0 percent of the labeled amount of hydrocortisone. It contains Acetic Acid, and may contain one or more suitable buffers, dispersants, and preservatives.
NOTE—Where Neomycin Sulfate and Hydrocortisone Otic Suspension is prescribed, without reference to the quantity of neomycin or hydrocortisone contained therein, a product containing 3.5 mg of neomycin and 10 mg of hydrocortisone per mL shall be dispensed.
Packaging and storage— Preserve in tight, light-resistant containers.
Sterility 71: meets the requirements.
pH 791: between 4.5 and 6.0.
Residual solvents 467: meets the requirements.
(Official January 1, 2007)
Assay for neomycin— Using an accurately measured volume of Otic Suspension, freshly mixed and free from entrapped air, proceed as directed in the Assay for neomycin under Neomycin and Polymyxin B Sulfates and Hydrocortisone Otic Solution.
Assay for hydrocortisone—
Mobile phase and Standard preparation—Prepare as directed in the Assay for hydrocortisone content under Neomycin and Polymyxin B Sulfates, Bacitracin Zinc, and Hydrocortisone Ophthalmic Ointment.
Assay preparation— Transfer 3.0 mL of Otic Suspension, freshly mixed and free from entrapped air, to a 200-mL volumetric flask, dilute with a mixture of methanol and water (1:1) to volume, and mix. Filter the solution, rejecting the first 10 mL of the filtrate.
Procedure— Proceed as directed for Procedure in the Assay for hydrocortisone content under Neomycin and Polymyxin B Sulfates, Bacitracin Zinc, and Hydrocortisone Ophthalmic Ointment. Calculate the quantity, in mg, of C21H30O5 in each mL of the Otic Suspension taken by the formula:
(66.67C)(rU / rS),
in which C is the concentration, in mg per mL, of USP Hydrocortisone RS in the Standard preparation, and rU and rS are the peak responses obtained from the Assay preparation and the Standard preparation, respectively.
Auxiliary Information— Staff Liaison : Brian D. Gilbert, Ph.D., Scientist
Expert Committee : (MDANT05) Monograph Development-Antibiotics
USP29–NF24 Page 1497
Phone Number : 1-301-816-8223