|
Daunorubicin Hydrochloride for Injection
» Daunorubicin Hydrochloride for Injection is a sterile mixture of Daunorubicin Hydrochloride and Mannitol. It contains the equivalent of not less than 90.0 percent and not more than 115.0 percent of the labeled amount of C27H29NO10.
Packaging and storage
Preserve in light-resistant Containers for Sterile Solids as described under Injections
Constituted solution
At the time of use, it meets the requirements for Constituted Solutions under Injections
Identification
The retention time of the main peak obtained with the Assay preparation corresponds to that obtained with the Standard preparation as directed in the Assay.
Bacterial endotoxins
pH
Water, Method I
Other requirements
It meets the requirements under Injections
Assay
Mobile phase, Standard preparation, Resolution solution, and Chromatographic system
Prepare as directed in the Assay under Daunorubicin Hydrochloride.
Assay preparation
Transfer the contents of 1 vial of Daunorubicin Hydrochloride for Injection with the aid of Mobile phase to an appropriate volumetric flask, and dilute with Mobile phase to volume to obtain a solution containing about 0.25 mg of daunorubicin per mL.
Procedure
Proceed as directed for Procedure in the Assay under Daunorubicin Hydrochloride. Calculate the quantity, in mg, of C27H29NO10 in the vial of Daunorubicin Hydrochloride for Injection taken by the formula:
(CV / 1000)(rU / rS)
in which V is the volume, in mL, of the Assay preparation, and the other terms are as defined therein.
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
Chromatographic Column
USP32NF27 Page 2061
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.
|