68071-2131-3 : NDC 2026 Code

68071-2131-3 : Bisoprolol Fumarate And Hydrochlorothiazide ( Bisoprolol Fumarate And Hydrochlorothiazide )

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NDC Code : 68071-2131-3 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68071-2131-3",
    "PackageDescription": "30 TABLET in 1 BOTTLE (68071-2131-3)",
    "NDC11Code": "68071-2131-03",
    "ProductNDC": "68071-2131",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Bisoprolol Fumarate And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Bisoprolol Fumarate And Hydrochlorothiazide",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20101012",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA079106",
    "LabelerName": "NuCare Pharmaceuticals, Inc.",
    "SubstanceName": "HYDROCHLOROTHIAZIDE; BISOPROLOL FUMARATE",
    "StrengthNumber": "6.25; 10",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-07-22",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}