51079-047-20 : NDC 2026 Code

51079-047-20 : Bupropion Hydrochloride ( Bupropion Hydrochloride )

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NDC Code : 51079-047-20 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51079-047-20",
    "PackageDescription": "100 BLISTER PACK in 1 CARTON (51079-047-20)  &gt; 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-047-01) ",
    "NDC11Code": "51079-0047-20",
    "ProductNDC": "51079-047",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bupropion Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bupropion Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20110323",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090942",
    "LabelerName": "Mylan Institutional Inc.",
    "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": "2019-12-24",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20110323",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}