{
"NDC": {
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"PackageDescription": "1 VIAL, MULTI-DOSE in 1 CARTON (83703-533-01) / 1 INJECTION in 1 VIAL, MULTI-DOSE",
"NDC11Code": "83703-0533-01",
"ProductNDC": "83703-533",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Bendamustine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Bendamustine Hydrochloride",
"DosageFormName": "INJECTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20221215",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA216078",
"LabelerName": "Bamboo US Bidco LCC",
"SubstanceName": "BENDAMUSTINE HYDROCHLORIDE",
"StrengthNumber": "100",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Alkylating Activity [MoA], Alkylating Drug [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-12-27",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20221215",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}