76420-907-01 : NDC 2026 Code

76420-907-01 : Lubiprostone ( Lubiprostone )

Additionally :

You can get information about “76420-907-01” NDC code in 76420-907-01 in HTML format

HTML | 76420-907-01 in TXT (Plain Text) format

TXT | 76420-907-01 in PDF (Portable Document Format)

PDF | 76420-907-01 in XML format

XML formats.

NDC Code : 76420-907-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "76420-907-01",
    "PackageDescription": "100 CAPSULE, GELATIN COATED in 1 BOTTLE (76420-907-01) ",
    "NDC11Code": "76420-0907-01",
    "ProductNDC": "76420-907",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Lubiprostone",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Lubiprostone",
    "DosageFormName": "CAPSULE, GELATIN COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20230101",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA021908",
    "LabelerName": "Asclemed USA, Inc.",
    "SubstanceName": "LUBIPROSTONE",
    "StrengthNumber": "24",
    "StrengthUnit": "ug/1",
    "Pharm_Classes": "Chloride Channel Activator [EPC], Chloride Channel Activators [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-01-29",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250128",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}