45865-520-49 : NDC 2025 Code

45865-520-49 : Benazepril Hydrochloride And Hydrochlorothiazide ( Benazepril Hydrochloride And Hydrochlorothiazide )

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NDC Code : 45865-520-49 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "45865-520-49",
    "PackageDescription": "100 TABLET, FILM COATED in 1 BOTTLE (45865-520-49)",
    "NDC11Code": "45865-0520-49",
    "ProductNDC": "45865-520",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Benazepril Hydrochloride And Hydrochlorothiazide",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Benazepril Hydrochloride And Hydrochlorothiazide",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20040211",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA076631",
    "LabelerName": "Medsource Pharmaceuticals",
    "SubstanceName": "BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE",
    "StrengthNumber": "20; 12.5",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-12-22",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20171231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}