{
"NDC": {
"NDCCode": "67457-325-12",
"PackageDescription": "5 mL in 1 VIAL, SINGLE-DOSE (67457-325-12) ",
"NDC11Code": "67457-0325-12",
"ProductNDC": "67457-325",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Bendamustine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Bendamustine Hydrochloride",
"DosageFormName": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20180426",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA204104",
"LabelerName": "Mylan Institutional LLC",
"SubstanceName": "BENDAMUSTINE HYDROCHLORIDE",
"StrengthNumber": "25",
"StrengthUnit": "mg/5mL",
"Pharm_Classes": "Alkylating Activity [MoA],Alkylating Drug [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-02-23",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20180426",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}