60687-723-21 : NDC 2026 Code

60687-723-21 : Duloxetine Hydrochloride ( Duloxetine )

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NDC Code : 60687-723-21 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-723-21",
    "PackageDescription": "30 BLISTER PACK in 1 CARTON (60687-723-21)  / 1 CAPSULE, DELAYED RELEASE in 1 BLISTER PACK (60687-723-11) ",
    "NDC11Code": "60687-0723-21",
    "ProductNDC": "60687-723",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Duloxetine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Duloxetine Hydrochloride",
    "DosageFormName": "CAPSULE, DELAYED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20230425",
    "EndMarketingDate": "20260531",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090778",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "DULOXETINE HYDROCHLORIDE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-04-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20230425",
    "EndMarketingDatePackage": "20260531",
    "SamplePackage": "N"
  }
}