55154-7889-0 : NDC 2026 Code

55154-7889-0 : Duloxetine Hydrochloride ( Duloxetine Hydrochloride )

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NDC Code : 55154-7889-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "55154-7889-0",
    "PackageDescription": "10 BLISTER PACK in 1 BAG (55154-7889-0)  &gt; 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK",
    "NDC11Code": "55154-7889-00",
    "ProductNDC": "55154-7889",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Duloxetine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Duloxetine Hydrochloride",
    "DosageFormName": "CAPSULE, DELAYED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20140613",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA202045",
    "LabelerName": "Cardinal Health",
    "SubstanceName": "DULOXETINE HYDROCHLORIDE",
    "StrengthNumber": "60",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2022-12-08",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20221231",
    "StartMarketingDatePackage": "20140613",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}