81033-149-52 : NDC 2026 Code

81033-149-52 : Sucralfate ( Sucralfate )

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NDC Code : 81033-149-52 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "81033-149-52",
    "PackageDescription": "100 CUP, UNIT-DOSE in 1 CASE (81033-149-52)  / 10 mL in 1 CUP, UNIT-DOSE (81033-149-10) ",
    "NDC11Code": "81033-0149-52",
    "ProductNDC": "81033-149",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Sucralfate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Sucralfate",
    "DosageFormName": "SUSPENSION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240701",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA216474",
    "LabelerName": "Kesin Pharma Corporation",
    "SubstanceName": "SUCRALFATE",
    "StrengthNumber": "1",
    "StrengthUnit": "g/10mL",
    "Pharm_Classes": "Aluminum Complex [EPC], Organometallic Compounds [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-06-07",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20240701",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}