60687-533-09 : NDC 2026 Code

60687-533-09 : Potassium Chloride ( Potassium Chloride )

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NDC Code : 60687-533-09 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-533-09",
    "PackageDescription": "80 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-533-09)  &gt; 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (60687-533-11) ",
    "NDC11Code": "60687-0533-09",
    "ProductNDC": "60687-533",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Potassium Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Potassium Chloride",
    "DosageFormName": "CAPSULE, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200227",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA202868",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "POTASSIUM CHLORIDE",
    "StrengthNumber": "750",
    "StrengthUnit": "mg/1",
    "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": "Deprecated",
    "LastUpdate": "2022-06-29",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20221231",
    "StartMarketingDatePackage": "20200227",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}