{
"NDC": {
"NDCCode": "68084-593-01",
"PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-593-01) > 1 TABLET in 1 BLISTER PACK (68084-593-11)",
"NDC11Code": "68084-0593-01",
"ProductNDC": "68084-593",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sucralfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sucralfate",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20120301",
"EndMarketingDate": "20161031",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074415",
"LabelerName": "American Health Packaging",
"SubstanceName": "SUCRALFATE",
"StrengthNumber": "1",
"StrengthUnit": "g/1",
"Pharm_Classes": "Aluminum Complex [EPC],Organometallic Compounds [Chemical/Ingredient]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2016-12-02",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}