70518-1002-1 : NDC 2026 Code

70518-1002-1 : Tenofovir Disoproxil Fumarate ( Tenofovir Disoproxil Fumarate )

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NDC Code : 70518-1002-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-1002-1",
    "PackageDescription": "4 TABLET in 1 BLISTER PACK (70518-1002-1) ",
    "NDC11Code": "70518-1002-01",
    "ProductNDC": "70518-1002",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Tenofovir Disoproxil Fumarate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Tenofovir Disoproxil Fumarate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20180202",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090742",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "TENOFOVIR DISOPROXIL FUMARATE",
    "StrengthNumber": "300",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Hepatitis B Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC],Nucleosides [CS],Nucleoside Reverse Transcriptase Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2021-04-30",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20211231",
    "StartMarketingDatePackage": "20190131",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}