50742-386-42 : NDC 2026 Code

50742-386-42 : Sucralfate ( Sucralfate )

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NDC Code : 50742-386-42 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50742-386-42",
    "PackageDescription": "420 mL in 1 BOTTLE (50742-386-42) ",
    "NDC11Code": "50742-0386-42",
    "ProductNDC": "50742-386",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Sucralfate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Sucralfate",
    "DosageFormName": "SUSPENSION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20241121",
    "EndMarketingDate": "20260731",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA216726",
    "LabelerName": "Ingenus Pharmaceuticals, LLC",
    "SubstanceName": "SUCRALFATE",
    "StrengthNumber": "1",
    "StrengthUnit": "g/10mL",
    "Pharm_Classes": "Aluminum Complex [EPC], Organometallic Compounds [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20241121",
    "EndMarketingDatePackage": "20260731",
    "SamplePackage": "N"
  }
}