51662-1387-1 : NDC 2026 Code

51662-1387-1 : Potassium Chloride ( Potassium Chloride )

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NDC Code : 51662-1387-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51662-1387-1",
    "PackageDescription": "10 mL in 1 VIAL, SINGLE-DOSE (51662-1387-1) ",
    "NDC11Code": "51662-1387-01",
    "ProductNDC": "51662-1387",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Potassium Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Potassium Chloride",
    "DosageFormName": "INJECTION, SOLUTION, CONCENTRATE",
    "RouteName": "INTRAVENOUS",
    "StartMarketingDate": "20191016",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA080205",
    "LabelerName": "HF Acquisition Co LLC, DBA HealthFirst",
    "SubstanceName": "POTASSIUM CHLORIDE",
    "StrengthNumber": "149",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-01-10",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20191016",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}