13811-715-90 : NDC 2026 Code

13811-715-90 : Venlafaxine Hydrochloride ( Venlafaxine Hydrochloride )

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NDC Code : 13811-715-90 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "13811-715-90",
    "PackageDescription": "90 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-715-90) ",
    "NDC11Code": "13811-0715-90",
    "ProductNDC": "13811-715",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Venlafaxine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Venlafaxine Hydrochloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20100429",
    "EndMarketingDate": "20260930",
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA022104",
    "LabelerName": "Trigen Laboratories, LLC",
    "SubstanceName": "VENLAFAXINE HYDROCHLORIDE",
    "StrengthNumber": "225",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-11-25",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20100429",
    "EndMarketingDatePackage": "20260330",
    "SamplePackage": "N"
  }
}