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55695-012-00 : NDC 2025 Code

55695-012-00 : Alendronate Sodium ( Alendronate Sodium )

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NDC Code : 55695-012-00 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "55695-012-00",
    "PackageDescription": "1 BLISTER PACK in 1 BOX, UNIT-DOSE (55695-012-00)  > 4 TABLET in 1 BLISTER PACK",
    "NDC11Code": "55695-0012-00",
    "ProductNDC": "55695-012",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Alendronate Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Alendronate Sodium",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20080804",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076984",
    "LabelerName": "Department of State Health Services, Pharmacy Branch",
    "SubstanceName": "ALENDRONATE SODIUM",
    "StrengthNumber": "70",
    "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
  }
}
                
            

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