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Penicillin G Benzathine Injectable Suspension
» Penicillin G Benzathine Injectable Suspension is a sterile suspension of Penicillin G Benzathine in Water for Injection with one or more suitable buffers, dispersants, preservatives, and suspending agents. It contains not less than 90.0 percent and not more than 115.0 percent of the labeled amount of penicillin.
Packaging and storage
Preserve in single-dose or multiple-dose containers, preferably of Type I or Type II glass, in a refrigerator.
USP Reference standards
USP Endotoxin RS. USP Penicillin G Benzathine RS. USP Penicillin G Potassium RS.
Identification
It responds to the Identification test under Penicillin G Benzathine Oral Suspension.
Bacterial endotoxins
Sterility
pH
Other requirements
It meets the requirements under Injections
Assay
Standard preparation
Using USP Penicillin G Potassium RS, prepare as directed for Standard preparation under Iodometric AssayAntibiotics
Assay preparation
Using a suitable hypodermic needle and syringe, withdraw an accurately measured volume of Injectable Suspension, equivalent to about 300,000 Penicillin G Units, and dilute quantitatively with 1.0 N sodium hydroxide to obtain an Assay preparation containing about 2000 Penicillin G Units per mL. Pipet 2.0 mL of this solution into a glass-stoppered, 125-mL conical flask.
Blank preparation
Using a suitable hypodermic needle and syringe, withdraw an accurately measured volume of Injectable Suspension, equivalent to about 300,000 Penicillin G Units, and quantitatively dilute with Buffer No. 1 to obtain a suspension containing about 2000 Penicillin G Units per mL. Pipet 2 mL of this solution into a glass-stoppered, 125-mL conical flask.
Procedure
Proceed as directed for Procedure under Iodometric AssayAntibiotics
(L / 2D)(F)(B
in which L is the labeled quantity, in Penicillin G Units per mL, in the Injectable Suspension taken, and D is the concentration, in Penicillin G Units per mL, in the Assay preparation on the basis of the labeled quantity in the Injectable Suspension and the extent of dilution, and the other terms are as defined therein.
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP32NF27 Page 3225
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