73159-008-60 : NDC 2026 Code

73159-008-60 : Halobetasol Propionate ( Ultravate )

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NDC Code : 73159-008-60 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "73159-008-60",
    "PackageDescription": "1 BOTTLE in 1 CARTON (73159-008-60)  / 59 g in 1 BOTTLE",
    "NDC11Code": "73159-0008-60",
    "ProductNDC": "73159-008",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ultravate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Halobetasol Propionate",
    "DosageFormName": "LOTION",
    "RouteName": "TOPICAL",
    "StartMarketingDate": "20250406",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA208183",
    "LabelerName": "Lacer Pharma, LLC",
    "SubstanceName": "HALOBETASOL PROPIONATE",
    "StrengthNumber": ".5",
    "StrengthUnit": "mg/g",
    "Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-05-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250406",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}