49884-735-82 : NDC 2026 Code

49884-735-82 : Fluoxetine Hydrochloride ( Fluoxetine Hydrochloride )

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NDC Code : 49884-735-82 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "49884-735-82",
    "PackageDescription": "2000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (49884-735-82)",
    "NDC11Code": "49884-0735-82",
    "ProductNDC": "49884-735",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fluoxetine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fluoxetine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20100113",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075755",
    "LabelerName": "Par Pharmaceutical, Inc",
    "SubstanceName": "FLUOXETINE HYDROCHLORIDE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2014-12-26",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}