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Erythromycin Injection
» Erythromycin Injection is a sterile solution of Erythromycin in a polyethylene glycol vehicle. It contains not less than 90.0 percent and not more than 120.0 percent of the labeled amount of C37H67NO13.
Packaging and storage
Preserve in multiple-dose containers.
Labeling
Label it to indicate that it is for veterinary use only. Label it to state that it is for intramuscular administration only.
Identification
Transfer a quantity of Injection, equivalent to about 5 mg of erythromycin, to a separator containing 50 mL of solvent hexane. Shake until dissolved. Extract with three separate 20-mL portions of methanol. Combine the methanol extracts in a beaker, and evaporate to dryness. Dissolve the residue in 2 mL of methanol (test solution). Proceed as directed in the Identification test under Erythromycin Delayed-Release Capsules, beginning with Prepare a Standard solution of USP Erythromycin RS.
Water, Method I
Sterility
Other requirements
It meets the requirements under Injections
Assay
Transfer an accurately measured volume of Injection, equivalent to about 50 mg of erythromycin, to a separator containing 50 mL of solvent hexane. Shake until dissolved. Wash with four separate 20-mL portions of a mixture of methanol and water (4:1). Combine the washings in a 100-mL volumetric flask, dilute with the methanol and water solution to volume, and mix. Proceed as directed for erythromycin under AntibioticsMicrobial Assays
Auxiliary Information
Please check for your question in the FAQs before contacting USP.
USP35NF30 Page 3080
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