68999-438-24 : NDC 2026 Code

68999-438-24 : Tricitrates ( Tricitrates )

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NDC Code : 68999-438-24 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68999-438-24",
    "PackageDescription": "2 TRAY in 1 BOX (68999-438-24)  / 10 CUP in 1 TRAY / 5 mL in 1 CUP (68999-438-05) ",
    "NDC11Code": "68999-0438-24",
    "ProductNDC": "68999-438",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Tricitrates",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Tricitrates",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20221208",
    "EndMarketingDate": null,
    "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
    "ApplicationNumber": null,
    "LabelerName": "Chartwell Governmental &amp; Specialty RX, LLC.",
    "SubstanceName": "CITRIC ACID MONOHYDRATE; POTASSIUM CITRATE; SODIUM CITRATE",
    "StrengthNumber": "334; 550; 500",
    "StrengthUnit": "mg/5mL; mg/5mL; mg/5mL",
    "Pharm_Classes": "Acidifying Activity [MoA], Acidifying Activity [MoA], Acidifying Activity [MoA], Anti-coagulant [EPC], Anti-coagulant [EPC], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE], Decreased Coagulation Factor Activity [PE]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-02-27",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260220",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}