Neomycin Sulfate Oral Solution
» Neomycin Sulfate Oral Solution contains the equivalent of not less than 90.0 percent and not more than 125.0 percent of the labeled amount of neomycin. It may contain one or more suitable colors, flavors, and preservatives.
Packaging and storage—
Preserve in tight, light-resistant containers, preferably at controlled room temperature.
USP Reference standards 
11
—
11—
USP Neomycin Sulfate RS
Thin-layer chromatographic identification test 201BNP:
meets the requirements.
201BNP:
meets the requirements.
Uniformity of dosage units 905—
905—
for oral solution packaged in single-unit containers:
meets the requirements.
Deliverable volume 698—
698—
for oral solution packaged in multiple-unit containers:
meets the requirements.
pH 791:
between 5.0 and 7.5.
791:
between 5.0 and 7.5.
Assay—
Proceed as directed under Antibiotics—Microbial Assays 81, using an accurately measured volume of Oral Solution quantitatively diluted with Buffer No. 3 to yield a solution having a convenient concentration of neomycin. Quantitatively dilute this stock solution with Buffer No. 3 to obtain a Test Dilution having a concentration assumed to be equal to the median dose level of the Standard.
81, using an accurately measured volume of Oral Solution quantitatively diluted with Buffer No. 3 to yield a solution having a convenient concentration of neomycin. Quantitatively dilute this stock solution with Buffer No. 3 to obtain a Test Dilution having a concentration assumed to be equal to the median dose level of the Standard.
Auxiliary Information—
Please check for your question in the FAQs before contacting USP.
| Topic/Question | Contact | Expert Committee |
|---|---|---|
| Monograph | Ahalya Wise, M.S.
Senior Scientific Liaison 1-301-816-8161 |
(SM12010) Monographs - Small Molecules 1 |
| Reference Standards | RS Technical Services 1-301-816-8129 rstech@usp.org |
USP35–NF30 Page 4011
Pharmacopeial Forum: Volume No. 30(1) Page 133