53217-321-01 : NDC 2026 Code

53217-321-01 : Alendronate Sodium ( Alendronate Sodium )

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NDC Code : 53217-321-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "53217-321-01",
    "PackageDescription": "4 TABLET in 1 BLISTER PACK (53217-321-01)",
    "NDC11Code": "53217-0321-01",
    "ProductNDC": "53217-321",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Alendronate Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Alendronate Sodium",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170501",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076984",
    "LabelerName": "Aidarex Pharmaceuticals LLC",
    "SubstanceName": "ALENDRONATE SODIUM",
    "StrengthNumber": "35",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Bisphosphonate [EPC],Diphosphonates [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-01-01",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}