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Technetium Tc 99m Medronate Injection
» Technetium Tc 99m Medronate Injection is a sterile, aqueous solution, suitable for intravenous administration, of sodium medronate and stannous chloride or stannous fluoride that is labeled with radioactive Tc 99m. It contains not less than 90.0 percent and not more than 110.0 percent of the labeled amount of Tc 99m as stannous medronate complex expressed in megabecquerels (microcuries or millicuries) per mL at the date and time indicated in the labeling. It may contain antimicrobial agents, antioxidants, and buffers. Other chemical forms of radioactivity do not exceed 10.0 percent of the total radioactivity.
Packaging and storage
Preserve in single-dose or multiple-dose containers at a temperature specified in the labeling.
USP Reference standards
USP Endotoxin RS
Bacterial endotoxins
pH
Radiochemical purity
Not more than 10.0% of unbound Tc 99m (free pertechnetate), hydrolyzed Tc 99m, and technetium-tin colloid is present, determined as follows.
System A
Under an atmosphere of nitrogen, place a measured volume of Injection, such that it provides a count rate of about 20,000 counts per minute, about 25 mm from one end of a paper chromatographic strip (see Chromatography
System B
Proceed as directed for System A, except to develop the chromatogram in dilute methanol (85 in 100). Free pertechnetate is located at an RF of 0.6 to 0.8. The sum of the percentage of radioactivity at the origin in System A plus the percentage of radioactivity at an RF of 0.6 to 0.8 in System B is not greater than 10.0%.
Other requirements
It meets the requirements of the tests for Radionuclide identification and Radionuclidic purity under Sodium Pertechnetate Tc 99m Injection, and meets the requirements for Labeling, Biological distribution, and Assay for radioactivity under Technetium Tc 99m Pyrophosphate Injection. It meets also the requirements under Injections
Auxiliary Information
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USP35NF30 Page 4767
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