70518-0122-5 : NDC 2026 Code

70518-0122-5 : Duloxetine Hydrochloride ( Duloxetine )

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NDC Code : 70518-0122-5 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-0122-5",
    "PackageDescription": "90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (70518-0122-5) ",
    "NDC11Code": "70518-0122-05",
    "ProductNDC": "70518-0122",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Duloxetine",
    "ProprietaryNameSuffix": "Delayed-release",
    "NonProprietaryName": "Duloxetine Hydrochloride",
    "DosageFormName": "CAPSULE, DELAYED RELEASE PELLETS",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170113",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA203088",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "DULOXETINE HYDROCHLORIDE",
    "StrengthNumber": "60",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-01-09",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20241002",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}