62034-021-77 : NDC 2026 Code

62034-021-77 : Duloxetine Hydrochloride ( Duloxetine )

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NDC Code : 62034-021-77 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "62034-021-77",
    "PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (62034-021-77)  &gt; 1 CAPSULE, DELAYED RELEASE PELLETS in 1 BLISTER PACK (62034-021-11)",
    "NDC11Code": "62034-0021-77",
    "ProductNDC": "62034-021",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Duloxetine",
    "ProprietaryNameSuffix": "Delayed-release",
    "NonProprietaryName": "Duloxetine Hydrochloride",
    "DosageFormName": "CAPSULE, DELAYED RELEASE PELLETS",
    "RouteName": "ORAL",
    "StartMarketingDate": "20160401",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA203088",
    "LabelerName": "Blenheim Pharmacal, Inc.",
    "SubstanceName": "DULOXETINE HYDROCHLORIDE",
    "StrengthNumber": "60",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-09-21",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}