0615-7799-39 : NDC 2026 Code

0615-7799-39 : Diazepam ( Diazepam )

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NDC Code : 0615-7799-39 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0615-7799-39",
    "PackageDescription": "30 TABLET in 1 BLISTER PACK (0615-7799-39) ",
    "NDC11Code": "00615-7799-39",
    "ProductNDC": "0615-7799",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Diazepam",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Diazepam",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "19861210",
    "EndMarketingDate": "20231031",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA071321",
    "LabelerName": "NCS HealthCare of KY, LLC dba Vangard Labs",
    "SubstanceName": "DIAZEPAM",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Benzodiazepine [EPC], Benzodiazepines [CS]",
    "DEASchedule": "CIV",
    "Status": "Deprecated",
    "LastUpdate": "2023-11-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20190311",
    "EndMarketingDatePackage": "20231031",
    "SamplePackage": "N"
  }
}