50268-141-15 : NDC 2026 Code

50268-141-15 : Bupropion Hydrochloride ( Bupropion Hydrochloride )

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NDC Code : 50268-141-15 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50268-141-15",
    "PackageDescription": "50 BLISTER PACK in 1 BOX (50268-141-15)  / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (50268-141-11) ",
    "NDC11Code": "50268-0141-15",
    "ProductNDC": "50268-141",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bupropion Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bupropion Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20161014",
    "EndMarketingDate": "20250131",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077284",
    "LabelerName": "AvPAK",
    "SubstanceName": "BUPROPION HYDROCHLORIDE",
    "StrengthNumber": "300",
    "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": "2025-02-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20161014",
    "EndMarketingDatePackage": "20250131",
    "SamplePackage": "N"
  }
}