{
"NDC": {
"NDCCode": "60505-0261-1",
"PackageDescription": "100 TABLET in 1 BOTTLE (60505-0261-1) ",
"NDC11Code": "60505-0261-01",
"ProductNDC": "60505-0261",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Benazepril Hydrochloride And Hydrochlorothiazide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Benazepril Hydrochloride And Hydrochlorothiazide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20140821",
"EndMarketingDate": "20260228",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078794",
"LabelerName": "Apotex Corp.",
"SubstanceName": "BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE",
"StrengthNumber": "5; 6.25",
"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 [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2026-03-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20140821",
"EndMarketingDatePackage": "20260228",
"SamplePackage": "N"
}
}