0615-8122-39 : NDC 2026 Code

0615-8122-39 : Venlafaxine Hydrochloride ( Venlafaxine Hydrochloride )

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NDC Code : 0615-8122-39 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0615-8122-39",
    "PackageDescription": "30 TABLET in 1 BLISTER PACK (0615-8122-39) ",
    "NDC11Code": "00615-8122-39",
    "ProductNDC": "0615-8122",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Venlafaxine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Venlafaxine Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20060804",
    "EndMarketingDate": "20220430",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076690",
    "LabelerName": "NCS HealthCare of KY, Inc dba Vangard Labs",
    "SubstanceName": "VENLAFAXINE HYDROCHLORIDE",
    "StrengthNumber": "75",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2022-05-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20180313",
    "EndMarketingDatePackage": "20220430",
    "SamplePackage": "N"
  }
}