81033-017-50 : NDC 2026 Code

81033-017-50 : Sodium Citrate And Citric Acid ( Sodium Citrate And Citric Acid )

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NDC Code : 81033-017-50 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "81033-017-50",
    "PackageDescription": "100 CUP, UNIT-DOSE in 1 CASE (81033-017-50)  / 15 mL in 1 CUP, UNIT-DOSE (81033-017-15) ",
    "NDC11Code": "81033-0017-50",
    "ProductNDC": "81033-017",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Sodium Citrate And Citric Acid",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Sodium Citrate And Citric Acid",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250401",
    "EndMarketingDate": null,
    "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
    "ApplicationNumber": null,
    "LabelerName": "Kesin Pharma Corporation",
    "SubstanceName": "ANHYDROUS CITRIC ACID; SODIUM CITRATE",
    "StrengthNumber": "334; 500",
    "StrengthUnit": "mg/5mL; mg/5mL",
    "Pharm_Classes": "Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-04-23",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250401",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}