50268-142-15 : NDC 2026 Code

50268-142-15 : Bupropion Hydrochloride ( Bupropion Hydrochloride )

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NDC Code : 50268-142-15 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50268-142-15",
    "PackageDescription": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-142-15)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-142-11) ",
    "NDC11Code": "50268-0142-15",
    "ProductNDC": "50268-142",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bupropion Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bupropion Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170802",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076143",
    "LabelerName": "AvPAK",
    "SubstanceName": "BUPROPION HYDROCHLORIDE",
    "StrengthNumber": "75",
    "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": "2026-02-25",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20170802",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}