24979-229-03 : NDC 2026 Code

24979-229-03 : Potassium Chloride ( Potassium Chloride )

Additionally :

You can get information about “24979-229-03” NDC code in 24979-229-03 in HTML format

HTML | 24979-229-03 in TXT (Plain Text) format

TXT | 24979-229-03 in PDF (Portable Document Format)

PDF | 24979-229-03 in XML format

XML formats.

NDC Code : 24979-229-03 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "24979-229-03",
    "PackageDescription": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (24979-229-03) ",
    "NDC11Code": "24979-0229-03",
    "ProductNDC": "24979-229",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Potassium Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Potassium Chloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20241028",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA218979",
    "LabelerName": "Upsher-Smith Laboratories, LLC",
    "SubstanceName": "POTASSIUM CHLORIDE",
    "StrengthNumber": "600",
    "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": "Active",
    "LastUpdate": "2025-05-07",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20241028",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}