60687-917-64 : NDC 2026 Code

60687-917-64 : Lactulose ( Lactulose )

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NDC Code : 60687-917-64 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-917-64",
    "PackageDescription": "4 TRAY in 1 CASE (60687-917-64)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-917-50)  / 15 mL in 1 CUP, UNIT-DOSE (60687-917-44) ",
    "NDC11Code": "60687-0917-64",
    "ProductNDC": "60687-917",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lactulose",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lactulose",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20260816",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090503",
    "LabelerName": "American Health Packaging",
    "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": "Active",
    "LastUpdate": "2026-08-25",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260816",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}