{
"NDC": {
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"PackageDescription": "30 TABLET, COATED in 1 BLISTER PACK (54458-893-10)",
"NDC11Code": "54458-0893-10",
"ProductNDC": "54458-893",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Benazepril",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Benazepril",
"DosageFormName": "TABLET, COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20130919",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076211",
"LabelerName": "International Laboratories, LLC",
"SubstanceName": "BENAZEPRIL HYDROCHLORIDE",
"StrengthNumber": "40",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-06-07",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}