70518-1192-1 : NDC 2026 Code

70518-1192-1 : Alendronate Sodium ( Alendronate Sodium )

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NDC Code : 70518-1192-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-1192-1",
    "PackageDescription": "3 BLISTER PACK in 1 CARTON (70518-1192-1)  / 4 TABLET in 1 BLISTER PACK",
    "NDC11Code": "70518-1192-01",
    "ProductNDC": "70518-1192",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Alendronate Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Alendronate Sodium",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20180516",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076768",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "ALENDRONATE SODIUM",
    "StrengthNumber": "35",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Bisphosphonate [EPC], Diphosphonates [CS]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-01-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20240112",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}