{
"NDC": {
"NDCCode": "51079-146-20",
"PackageDescription": "100 BLISTER PACK in 1 CARTON (51079-146-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-146-01) ",
"NDC11Code": "51079-0146-20",
"ProductNDC": "51079-146",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Benazepril Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Benazepril Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20040521",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076430",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "BENAZEPRIL HYDROCHLORIDE",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20040521",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}