70518-0639-0 : NDC 2026 Code

70518-0639-0 : Bupropion Hydrochloride ( Wellbutrin )

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NDC Code : 70518-0639-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-0639-0",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0639-0) ",
    "NDC11Code": "70518-0639-00",
    "ProductNDC": "70518-0639",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Wellbutrin",
    "ProprietaryNameSuffix": "Sr",
    "NonProprietaryName": "Bupropion Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170725",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA020358",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "BUPROPION HYDROCHLORIDE",
    "StrengthNumber": "100",
    "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": "2020-04-09",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": "20170725",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}