51079-482-56 : NDC 2026 Code

51079-482-56 : Venlafaxine Hydrochloride ( Venlafaxine Hydrochloride )

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NDC Code : 51079-482-56 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51079-482-56",
    "PackageDescription": "10 DOSE PACK in 1 CARTON (51079-482-56)  &gt; 30 BLISTER PACK in 1 DOSE PACK (51079-482-30)  &gt; 1 TABLET in 1 BLISTER PACK (51079-482-01) ",
    "NDC11Code": "51079-0482-56",
    "ProductNDC": "51079-482",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Venlafaxine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Venlafaxine Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20080715",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077166",
    "LabelerName": "Mylan Institutional Inc.",
    "SubstanceName": "VENLAFAXINE HYDROCHLORIDE",
    "StrengthNumber": "75",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20091201",
    "EndMarketingDatePackage": "20181231",
    "SamplePackage": "N"
  }
}