24658-163-73 : NDC 2026 Code

24658-163-73 : Alendronate Sodium ( Alendronate Sodium )

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NDC Code : 24658-163-73 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "24658-163-73",
    "PackageDescription": "3 BLISTER PACK in 1 CARTON (24658-163-73)  &gt; 4 TABLET in 1 BLISTER PACK (24658-163-71)",
    "NDC11Code": "24658-0163-73",
    "ProductNDC": "24658-163",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Alendronate Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Alendronate Sodium",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20130205",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090258",
    "LabelerName": "Blu Pharmaceuticals, LLC",
    "SubstanceName": "ALENDRONATE SODIUM",
    "StrengthNumber": "70",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2016-12-02",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}