» Chloramphenicol Injection is a sterile solution of Chloramphenicol in one or more suitable solvents. It contains not less than 90.0 percent and not more than 115.0 percent of the labeled amount of C11H12Cl2N2O5. It may contain suitable buffers.
Packaging and storage Preserve in single-dose or in multiple-dose containers.
Labeling Label it to indicate that it is for veterinary use only.
Identification 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.
Bacterial endotoxins 85 It contains not more than 0.2 USP Endotoxin Unit per mg of chloramphenicol.
Sterility 71 It meets the requirements when tested as directed for Membrane Filtration under Test for Sterility of the Product to be Examined, 1 mL from each container being transferred directly to the membrane filter.
pH 791: between 5.0 and 8.0, in a solution diluted with water (1:1).
Other requirements It meets the requirements under Injections 1.
Mobile phase, Standard preparation, and Chromatographic system Prepare as directed in the Assay under Chloramphenicol.
Assay preparation Transfer an accurately measured volume of Chloramphenicol Injection, equivalent to about 200 mg of chloramphenicol, to a 100-mL volumetric flask, add Mobile phase to volume, and mix. Transfer 4.0 mL of the resulting solution to a 100-mL volumetric flask, dilute with Mobile phase to volume, and mix. Filter this solution through a 0.5-µm or finer porosity filter.
Auxiliary Information Please check for your question in the FAQs before contacting USP.Chromatographic Column
USP32NF27 Page 1886
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.