52125-732-17 : NDC 2026 Code

52125-732-17 : Alendronate Sodium ( Alendronate Sodium )

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NDC Code : 52125-732-17 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "52125-732-17",
    "PackageDescription": "4 TABLET in 1 BOX (52125-732-17)",
    "NDC11Code": "52125-0732-17",
    "ProductNDC": "52125-732",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Alendronate Sodium",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Alendronate Sodium",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20131007",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075710",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "ALENDRONATE SODIUM",
    "StrengthNumber": "35",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-01-02",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}