{
"NDC": {
"NDCCode": "52125-770-19",
"PackageDescription": "90 TABLET in 1 BOTTLE (52125-770-19)",
"NDC11Code": "52125-0770-19",
"ProductNDC": "52125-770",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Enalapril Maleate And Hydrochlorothiazide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Enalapril Maleate And Hydrochlorothiazide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20131112",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076486",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE",
"StrengthNumber": "5; 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": "2016-12-27",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}