61919-063-72 : NDC 2026 Code

61919-063-72 : Bupropion Hydrochloride ( Bupropion Hydrochloride )

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NDC Code : 61919-063-72 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "61919-063-72",
    "PackageDescription": "120 TABLET, EXTENDED RELEASE in 1 BOTTLE (61919-063-72)",
    "NDC11Code": "61919-0063-72",
    "ProductNDC": "61919-063",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bupropion Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bupropion Hydrochloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170216",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075932",
    "LabelerName": "DIRECT RX",
    "SubstanceName": "BUPROPION HYDROCHLORIDE",
    "StrengthNumber": "150",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-09-21",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "E",
    "ListingRecordCertifiedThrough": "20181231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}