51672-5306-2 : NDC 2026 Code

51672-5306-2 : Fluoxetine Hydrochloride ( Fluoxetine Hydrochloride )

Additionally :

You can get information about “51672-5306-2” NDC code in 51672-5306-2 in HTML format

HTML | 51672-5306-2 in TXT (Plain Text) format

TXT | 51672-5306-2 in PDF (Portable Document Format)

PDF | 51672-5306-2 in XML format

XML formats.

NDC Code : 51672-5306-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51672-5306-2",
    "PackageDescription": "500 TABLET, FILM COATED in 1 BOTTLE (51672-5306-2) ",
    "NDC11Code": "51672-5306-02",
    "ProductNDC": "51672-5306",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Fluoxetine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Fluoxetine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20190215",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211477",
    "LabelerName": "Taro Pharmaceuticals U.S.A., Inc.",
    "SubstanceName": "FLUOXETINE HYDROCHLORIDE",
    "StrengthNumber": "60",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-03-12",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20190215",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}