{
"NDC": {
"NDCCode": "59762-1736-2",
"PackageDescription": "100 TABLET in 1 BOTTLE (59762-1736-2)",
"NDC11Code": "59762-1736-02",
"ProductNDC": "59762-1736",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Hydrochlorothiazide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Hydrochlorothiazide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20070720",
"EndMarketingDate": "20140630",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040780",
"LabelerName": "Greenstone LLC",
"SubstanceName": "HYDROCHLOROTHIAZIDE",
"StrengthNumber": "25",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2014-07-07",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}