Cloxacillin Benzathine Intramammary Infusion
»Cloxacillin Benzathine Intramammary Infusion is a suspension of Cloxacillin Benzathine in a suitable oil vehicle.It has a potency equivalent to not less than 90.0percent and not more than 120.0percent of the labeled amount of cloxacillin (C19H18ClN3O5S).
Packaging and storage— Preserve in disposable syringes that are well-closed containers,except that where the Intramammary Infusion is labeled as sterile,the individual syringes or cartons are sealed and tamper-proof so that sterility is assured at time of use.
Labeling— Label it to indicate that it is for veterinary use only.Intramammary Infusion that is sterile may be so labeled.
Identification,Infrared Absorption á197Kñ Obtain the test specimen as follows.Transfer a quantity of Intramammary Infusion,equivalent to about 500mg of cloxacillin,to a 50-mLcentrifuge tube,add 25mLof toluene,mix,and centrifuge.Decant and discard the toluene.Wash the residue with four 25-mLportions of toluene,sonicating for about 30seconds after each addition of toluene.Dry the residue in vacuum over silica gel.
Sterility á71ñ(where labeled as being sterile)— It meets the requirements when tested as directed for Direct Inoculation of the Culture Mediumunder Test for Sterility of the Product to be Examined,except to use Fluid Thioglycollate Medium containing polysorbate 80solution (1in 200)and an amount of sterile penicillinase sufficient to inactivate the cloxacillin in each tube,to use Soybean–Casein Digest Medium containing polysorbate 80solution (1in 200)and an amount of sterile penicillinase sufficient to inactivate the cloxacillin in each tube,and to shake the tubes once daily.
Water,Method Iá921ñ: not more than 1.0%,20mLof a mixture of toluene and methanol (7:3)being used in place of methanol in the titration vessel.
Assay— Proceed as directed for cloxacillin under Antibiotics—Microbial Assays á81ñ,expelling the contents of 1syringe of Intramammary Infusion into a high-speed glass blender jar containing sufficient methanol to yield a volume of 500mL,and blend for 3to 5minutes.Promptly dilute an accurately measured volume of this solution quantitatively and stepwise with Buffer No.1to obtain a Test Dilutionhaving a concentration assumed to be equal to the median dose level of the Standard.
Auxiliary Information— Staff Liaison:Ian DeVeau,Ph.D.,Senior Scientist
Expert Committee:(VET)Veterinary Drugs
USP28–NF23Page 525
Phone Number:1-301-816-8178