{
"NDC": {
"NDCCode": "47335-937-40",
"PackageDescription": "1 VIAL, SINGLE-DOSE in 1 CARTON (47335-937-40) > 2 mL in 1 VIAL, SINGLE-DOSE",
"NDC11Code": "47335-0937-40",
"ProductNDC": "47335-937",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Irinotecan Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Irinotecan Hydrochloride",
"DosageFormName": "INJECTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20080421",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078805",
"LabelerName": "Sun Pharma Global FZE",
"SubstanceName": "IRINOTECAN HYDROCHLORIDE",
"StrengthNumber": "40",
"StrengthUnit": "mg/2mL",
"Pharm_Classes": "Topoisomerase Inhibitor [EPC],Topoisomerase Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-01-30",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}