{
"NDC": {
"NDCCode": "55390-139-10",
"PackageDescription": "1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (55390-139-10)",
"NDC11Code": "55390-0139-10",
"ProductNDC": "55390-139",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Polymyxin B",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Polymyxin B Sulfate",
"DosageFormName": "INJECTION, POWDER, FOR SOLUTION",
"RouteName": "INTRAMUSCULAR; INTRATHECAL; INTRAVENOUS; OPHTHALMIC",
"StartMarketingDate": "19980601",
"EndMarketingDate": "20140331",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA060716",
"LabelerName": "Bedford Laboratories",
"SubstanceName": "POLYMYXIN B SULFATE",
"StrengthNumber": "500000",
"StrengthUnit": "[iU]/1",
"Pharm_Classes": "Polymyxin-class Antibacterial [EPC],Polymyxins [Chemical/Ingredient]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2014-04-03",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}