70934-761-90 : NDC 2026 Code

70934-761-90 : Venlafaxine ( Venlafaxine )

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NDC Code : 70934-761-90 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70934-761-90",
    "PackageDescription": "90 TABLET in 1 BOTTLE, PLASTIC (70934-761-90) ",
    "NDC11Code": "70934-0761-90",
    "ProductNDC": "70934-761",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Venlafaxine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Venlafaxine",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200529",
    "EndMarketingDate": "20240831",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078932",
    "LabelerName": "Denton Pharma, Inc. DBA Northwind Pharmaceuticals",
    "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": "2024-09-03",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20200529",
    "EndMarketingDatePackage": "20240831",
    "SamplePackage": "N"
  }
}