81033-220-52 : NDC 2026 Code

81033-220-52 : Potassium Chloride ( Potassium Chloride )

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NDC Code : 81033-220-52 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "81033-220-52",
    "PackageDescription": "5 TRAY in 1 CASE (81033-220-52)  / 10 CUP, UNIT-DOSE in 1 TRAY / 15 mL in 1 CUP, UNIT-DOSE (81033-220-15) ",
    "NDC11Code": "81033-0220-52",
    "ProductNDC": "81033-220",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Potassium Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Potassium Chloride",
    "DosageFormName": "SOLUTION",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220815",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211648",
    "LabelerName": "Kesin Pharma Corporation",
    "SubstanceName": "POTASSIUM CHLORIDE",
    "StrengthNumber": "1.5",
    "StrengthUnit": "g/15mL",
    "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": "2024-03-14",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20220815",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}