60687-834-76 : NDC 2026 Code

60687-834-76 : Sodium Citrate And Citric Acid Monohydrate ( Sodium Citrate And Citric Acid )

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NDC Code : 60687-834-76 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-834-76",
    "PackageDescription": "10 TRAY in 1 CASE (60687-834-76)  / 10 CUP, UNIT-DOSE in 1 TRAY (60687-834-51)  / 30 mL in 1 CUP, UNIT-DOSE (60687-834-45) ",
    "NDC11Code": "60687-0834-76",
    "ProductNDC": "60687-834",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Sodium Citrate And Citric Acid",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Sodium Citrate And Citric Acid Monohydrate",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240721",
    "EndMarketingDate": null,
    "MarketingCategoryName": "UNAPPROVED DRUG OTHER",
    "ApplicationNumber": null,
    "LabelerName": "American Health Packaging",
    "SubstanceName": "ANHYDROUS CITRIC ACID; SODIUM CITRATE, UNSPECIFIED FORM",
    "StrengthNumber": "2004; 3000",
    "StrengthUnit": "mg/30mL; mg/30mL",
    "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": "2024-07-23",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20240721",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}