51672-4219-1 : NDC 2026 Code

51672-4219-1 : Doxepin Hydrochloride ( Doxepin Hydrochloride )

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NDC Code : 51672-4219-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51672-4219-1",
    "PackageDescription": "100 CAPSULE in 1 BOTTLE (51672-4219-1) ",
    "NDC11Code": "51672-4219-01",
    "ProductNDC": "51672-4219",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Doxepin Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Doxepin Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200701",
    "EndMarketingDate": "20260331",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA213063",
    "LabelerName": "Sun Pharmaceutical Industries, Inc.",
    "SubstanceName": "DOXEPIN HYDROCHLORIDE",
    "StrengthNumber": "50",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Tricyclic Antidepressant [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2026-02-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20200701",
    "EndMarketingDatePackage": "20260131",
    "SamplePackage": "N"
  }
}