83008-082-30 : NDC 2026 Code

83008-082-30 : Bupropion Hydrochloride ( Bupropion Hydrochloride )

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NDC Code : 83008-082-30 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "83008-082-30",
    "PackageDescription": "30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (83008-082-30) ",
    "NDC11Code": "83008-0082-30",
    "ProductNDC": "83008-082",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bupropion Hydrochloride",
    "ProprietaryNameSuffix": "(xl)",
    "NonProprietaryName": "Bupropion Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20240828",
    "EndMarketingDate": "20261231",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA207479",
    "LabelerName": "Quality Care Products, LLC",
    "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": "Active",
    "LastUpdate": "2024-12-27",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20240828",
    "EndMarketingDatePackage": "20261231",
    "SamplePackage": "N"
  }
}