68084-552-21 : NDC 2025 Code

68084-552-21 : Ketoconazole ( Ketoconazole )

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NDC Code : 68084-552-21 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68084-552-21",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-552-21)  &gt; 1 TABLET in 1 BLISTER PACK (68084-552-11) ",
    "NDC11Code": "68084-0552-21",
    "ProductNDC": "68084-552",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ketoconazole",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ketoconazole",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20111221",
    "EndMarketingDate": "20190531",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075597",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "KETOCONAZOLE",
    "StrengthNumber": "200",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Azole Antifungal [EPC],Azoles [CS],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A5 Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-06-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20111221",
    "EndMarketingDatePackage": "20190531",
    "SamplePackage": "N"
  }
}