51079-971-19 : NDC 2026 Code

51079-971-19 : Fluoxetine Hydrochloride ( Fluoxetine )

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NDC Code : 51079-971-19 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51079-971-19",
    "PackageDescription": "25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-971-19)  &gt; 1 CAPSULE in 1 BLISTER PACK (51079-971-17)",
    "NDC11Code": "51079-0971-19",
    "ProductNDC": "51079-971",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fluoxetine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fluoxetine Hydrochloride",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20110711",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075207",
    "LabelerName": "UDL Laboratories, Inc.",
    "SubstanceName": "FLUOXETINE HYDROCHLORIDE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2014-02-10",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}