{
"NDC": {
"NDCCode": "55154-9448-5",
"PackageDescription": "5 CUP, UNIT-DOSE in 1 BAG (55154-9448-5) / 30 mL in 1 CUP, UNIT-DOSE",
"NDC11Code": "55154-9448-05",
"ProductNDC": "55154-9448",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Lactulose",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lactulose",
"DosageFormName": "SOLUTION",
"RouteName": "ORAL",
"StartMarketingDate": "19660730",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074623",
"LabelerName": "Cardinal Health 107, LLC",
"SubstanceName": "LACTULOSE",
"StrengthNumber": "20",
"StrengthUnit": "g/30mL",
"Pharm_Classes": "Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-01-23",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "19660730",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}