68084-538-25 : NDC 2025 Code

68084-538-25 : Voriconazole ( Voriconazole )

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NDC Code : 68084-538-25 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68084-538-25",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-538-25)  &gt; 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-538-95)",
    "NDC11Code": "68084-0538-25",
    "ProductNDC": "68084-538",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Voriconazole",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Voriconazole",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20120501",
    "EndMarketingDate": "20180731",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA200265",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "VORICONAZOLE",
    "StrengthNumber": "200",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Azole Antifungal [EPC],Azoles [Chemical/Ingredient],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2018-07-31",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}