{
"NDC": {
"NDCCode": "51079-072-56",
"PackageDescription": "10 DOSE PACK in 1 CARTON (51079-072-56) > 30 BLISTER PACK in 1 DOSE PACK (51079-072-30) > 1 TABLET in 1 BLISTER PACK (51079-072-01) ",
"NDC11Code": "51079-0072-56",
"ProductNDC": "51079-072",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Furosemide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Furosemide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "19951001",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA018487",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "FUROSEMIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Increased Diuresis at Loop of Henle [PE],Loop Diuretic [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-04-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20070801",
"EndMarketingDatePackage": "20190331",
"SamplePackage": "N"
}
}