{
"NDC": {
"NDCCode": "43602-548-05",
"PackageDescription": "500 CAPSULE in 1 BOTTLE (43602-548-05) ",
"NDC11Code": "43602-0548-05",
"ProductNDC": "43602-548",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Lubiprostone",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lubiprostone",
"DosageFormName": "CAPSULE",
"RouteName": "ORAL",
"StartMarketingDate": "20250102",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA218640",
"LabelerName": "Ascent Pharmaceuticals, Inc.",
"SubstanceName": "LUBIPROSTONE",
"StrengthNumber": ".008",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Chloride Channel Activator [EPC], Chloride Channel Activators [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2025-10-09",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20250102",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}