Polymyxin B for Injection
» Polymyxin B for Injection contains an amount of Polymyxin B Sulfate equivalent to not less than 90.0 percent and not more than 120.0 percent of the labeled amount of polymyxin B.
Packaging and storage
Preserve in Containers for Sterile Solids as described under Injections 1, protected from light.
Labeling
Label it to indicate that where it is administered intramuscularly and/or intrathecally, it is to be given only to patients hospitalized so as to provide constant supervision by a physician.
Constituted solution
At the time of use, it meets the requirements for Constituted Solutions under Injections 1.
Thin-layer chromatographic identification test 201BNP:
meets the requirements.
Pyrogen
It meets the requirements of the Pyrogen Test 151, the test dose being 1.0 mL per kg of a solution in pyrogen-free saline TS containing 20,000 Polymyxin B Units per mL.
Sterility 71
It meets the requirements when tested as directed for Membrane Filtration under Test for Sterility of the Product to be Examined.
Particulate matter 788:
meets the requirements for small-volume injections.
Residue on ignition 281:
not more than 5.0%, the charred residue being moistened with 2 mL of nitric acid and 5 drops of sulfuric acid.
Heavy metals, Method II 231:
not more than 0.01%.
Other requirements
It meets the requirements for pH and Loss on drying under Polymyxin B Sulfate. It also meets the requirements for Uniformity of Dosage Units 905 and for Labeling under Injections 1.
Assay
Assay preparation 1
(where it is represented as being in a single-dose container)Constitute Polymyxin B for Injection in a volume of water, accurately measured, corresponding to the volume of solvent specified in the labeling. Withdraw all of the withdrawable contents, using a suitable hypodermic needle and syringe, and dilute quantitatively with Buffer No. 6 to obtain a solution containing a convenient number of Polymyxin B Units per mL.
Assay preparation 2
(where the label states the quantity of polymyxin B in a given volume of constituted solution)Constitute 1 container of Polymyxin B for Injection in a volume of water, accurately measured, corresponding to the volume of solvent specified in the labeling. Dilute an accurately measured volume of the constituted solution quantitatively with Buffer No. 6 to obtain a solution containing a convenient number of Polymyxin B Units per mL.
Procedure
Proceed as directed under AntibioticsMicrobial Assays 81, using an accurately measured volume of Assay preparation diluted quantitatively with Buffer No. 6 to yield a Test Dilution having a concentration assumed to be equal to the median dose level of the Standard.
Auxiliary Information
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USP32NF27 Page 3326
Pharmacopeial Forum: Volume No. 28(4) Page 1184
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