{
"NDC": {
"NDCCode": "55154-4055-5",
"PackageDescription": "5 CUP, UNIT-DOSE in 1 BAG (55154-4055-5) > 30 mL in 1 CUP, UNIT-DOSE",
"NDC11Code": "55154-4055-05",
"ProductNDC": "55154-4055",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Lactulose",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lactulose",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "20100510",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074138",
"LabelerName": "Cardinal Health",
"SubstanceName": "LACTULOSE",
"StrengthNumber": "20",
"StrengthUnit": "g/30mL",
"Pharm_Classes": "Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-02-02",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20171231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}