{
"NDC": {
"NDCCode": "68071-4421-3",
"PackageDescription": "30 TABLET in 1 BOTTLE (68071-4421-3) ",
"NDC11Code": "68071-4421-03",
"ProductNDC": "68071-4421",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Gemfibrozil",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Gemfibrozil",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20170215",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA203266",
"LabelerName": "NuCare Pharmaceuticals,Inc.",
"SubstanceName": "GEMFIBROZIL",
"StrengthNumber": "600",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Peroxisome Proliferator-activated Receptor alpha Agonists [MoA],PPAR alpha [CS],Peroxisome Proliferator Receptor alpha Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20180508",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}