» Phenylbutazone Injection is a sterile solution of Phenylbutazone in Sterile Water for Injection. It contains not less than 90.0 percent and not more than 110.0 percent of the labeled amount of C19H20N2O2.
Packaging and storage Preserve in single-dose or multiple-dose containers, preferably of Type I glass. Protect from light, and store in a refrigerator.
Labeling Label Injection to indicate that it is for veterinary use only.
Clarity of solution The Injection is essentially free from particles of foreign matter that can be observed on visual inspection.
A: Transfer a volume of Injection, equivalent to about 500 mg of phenylbutazone, to a 250-mL conical flask, add 100 mL of solvent hexane, and heat the mixture under reflux for 15 minutes. Filter the hot mixture, and allow the filtrate to cool. Separate the crystals thus formed by filtration, and dry in vacuum at 80 for 30 minutes: the phenylbutazone so obtained responds to Identification test A under Phenylbutazone.
B: The retention time of the phenylbutazone peak in the chromatogram of the Assay preparation corresponds to that in the chromatogram of the Standard preparation as obtained in the Assay.
Sterility 71 It meets the requirements when tested as directed for Membrane Filtration under Test for Sterility of the Product to be Examined.
Bacterial endotoxins 85 It contains not more than 1.1 USP Endotoxin Units per mg of phenylbutazone.
pH 791: between 9.5 and 10.0.
Other requirements It meets the requirements under Injections 1.
Acetate buffer, Mobile phase, Internal standard solution, Standard preparation, and Chromatographic system Proceed as directed in the Assay under Phenylbutazone.
Assay preparation Transfer an accurately measured volume of Injection, equivalent to about 200 mg of phenylbutazone, to a 100-mL volumetric flask. Dilute with acetonitrile to volume, and mix. Transfer 7.0 mL of this solution to a 50-mL volumetric flask, add 10.0 mL of Internal standard solution, dilute with acetonitrile to volume, and mix. [noteUse this solution within 8 hours of its preparation.]
Procedure Proceed as directed for Procedure in the Assay under Phenylbutazone. Calculate the quantity, in mg, of C19H20N2O2 in each mL of the Injection taken by the formula:
350(C / V)(RU / RS)in which C is the concentration, in mg per mL, of USP Phenylbutazone RS in the Standard preparation, V is the volume, in mL, of Injection taken to prepare the Assay preparation, and RU and RS are the ratios of the peak responses of phenylbutazone to that of the internal standard obtained from the Assay preparation and the Standard preparation, respectively.
Auxiliary Information Please check for your question in the FAQs before contacting USP.Chromatographic Column
USP32NF27 Page 3282Pharmacopeial Forum: Volume No. 29(6) Page 1964
Chromatographic columns text is not derived from, and not part of, USP 32 or NF 27.