50090-6478-0 : NDC 2026 Code

50090-6478-0 : Bisoprolol Fumarate And Hydrochlorothiazide ( Bisoprolol Fumarate And Hydrochlorothiazide )

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NDC Code : 50090-6478-0 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50090-6478-0",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (50090-6478-0) ",
    "NDC11Code": "50090-6478-00",
    "ProductNDC": "50090-6478",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bisoprolol Fumarate And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bisoprolol Fumarate And Hydrochlorothiazide",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20190807",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA AUTHORIZED GENERIC",
    "ApplicationNumber": "NDA020186",
    "LabelerName": "A-S Medication Solutions",
    "SubstanceName": "BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE",
    "StrengthNumber": "2.5; 6.25",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2023-05-25",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20230516",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}