72789-202-01 : NDC 2026 Code

72789-202-01 : Potassium Citrate ( Potassium Citrate )

Additionally :

You can get information about “72789-202-01” NDC code in 72789-202-01 in HTML format

HTML | 72789-202-01 in TXT (Plain Text) format

TXT | 72789-202-01 in PDF (Portable Document Format)

PDF | 72789-202-01 in XML format

XML formats.

NDC Code : 72789-202-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "72789-202-01",
    "PackageDescription": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-202-01) ",
    "NDC11Code": "72789-0202-01",
    "ProductNDC": "72789-202",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Potassium Citrate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Potassium Citrate",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20210301",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA214426",
    "LabelerName": "PD-Rx Pharmaceuticals, Inc.",
    "SubstanceName": "POTASSIUM CITRATE",
    "StrengthNumber": "5",
    "StrengthUnit": "meq/1",
    "Pharm_Classes": "Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2024-10-11",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20251231",
    "StartMarketingDatePackage": "20210923",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}