{
"NDC": {
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"PackageDescription": "10 BLISTER PACK in 1 BAG (55154-5673-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK",
"NDC11Code": "55154-5673-00",
"ProductNDC": "55154-5673",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
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"ProprietaryNameSuffix": null,
"NonProprietaryName": "Benazepril Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20040521",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076430",
"LabelerName": "Cardinal Health",
"SubstanceName": "BENAZEPRIL HYDROCHLORIDE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-05-28",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20040521",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}