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Ticarcillin for Injection
» Ticarcillin for Injection contains an amount of Ticarcillin Disodium equivalent to not less than 90.0 percent and not more than 115.0 percent of the labeled amount of ticarcillin (C15H16N2O6S2).
Packaging and storage
Preserve in Containers for Sterile Solids as described under Injections
USP Reference standards
USP Endotoxin RS
Constituted solution
At the time of use, it meets the requirements for Constituted Solutions under Injections
Bacterial endotoxins
Sterility
pH
Water, Method I
Particulate matter
Other requirements
It responds to the Identification tests and meets the requirements for Water and Dimethylaniline under Ticarcillin Disodium. It meets also the requirements for Uniformity of Dosage Units
Assay
pH 4.3 sodium phosphate buffer, Mobile phase, pH 6.4 sodium phosphate buffer, Standard preparation, Resolution solution, and Chromatographic system
Proceed as directed in the Assay under Ticarcillin Monosodium.
Assay preparation 1
(where it is represented as being in a single-dose container)Constitute Ticarcillin for Injection as directed in the labeling. Withdraw all of the withdrawable contents, and dilute quantitatively with pH 6.4 sodium phosphate buffer to obtain a solution having a concentration of about 0.9 mg of ticarcillin (C15H16N2O6S2) per mL.
Assay preparation 2
(where the label states the quantity of ticarcillin in a given volume of constituted solution)Constitute Ticarcillin for Injection as directed in the labeling. Dilute an accurately measured volume of the constituted solution quantitatively with pH 6.4 sodium phosphate buffer to obtain a solution having a concentration of about 0.9 mg of ticarcillin (C15H16N2O6S2) per mL.
Procedure
Proceed as directed for Procedure in the Assay under Ticarcillin Monosodium. Calculate the quantity, in mg, of ticarcillin (C15H16N2O6S2) withdrawn from the container or in the volume of constituted solution taken by the formula:
(L / D)(CP / 1000)(rU / rS)
in which L is the labeled quantity, in mg per mL, of ticarcillin (C15H16N2O6S2) in the container or in the volume of constituted solution taken; D is the concentration, in mg per mL, of ticarcillin in Assay preparation 1 or Assay preparation 2, based on the labeled quantity in the container or in the portion of constituted solution taken, and the extent of dilution; C is the concentration, in mg per mL, of USP Ticarcillin Monosodium Monohydrate RS in the Standard preparation; P is the designated potency, in µg of ticarcillin per mg, of USP Ticarcillin Monosodium Monohydrate RS; and rU and rS are the ticarcillin peak responses obtained from the Assay preparation and the Standard preparation, respectively.
Auxiliary Information
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USP35NF30 Page 4862
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