{
"NDC": {
"NDCCode": "80432-068-35",
"PackageDescription": "946 mL in 1 BOTTLE (80432-068-35) ",
"NDC11Code": "80432-0068-35",
"ProductNDC": "80432-068",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Lactulose",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lactulose",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20241210",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA074623",
"LabelerName": "TriRx Huntsville Pharmaceutical Services",
"SubstanceName": "LACTULOSE",
"StrengthNumber": "10",
"StrengthUnit": "g/15mL",
"Pharm_Classes": "Acidifying Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-01-04",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20241210",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}