{
"NDC": {
"NDCCode": "60687-284-21",
"PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-284-21) > 1 TABLET in 1 BLISTER PACK (60687-284-11) ",
"NDC11Code": "60687-0284-21",
"ProductNDC": "60687-284",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ezetimibe",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ezetimibe",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20170126",
"EndMarketingDate": "20190930",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078560",
"LabelerName": "American Health Packaging",
"SubstanceName": "EZETIMIBE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Decreased Cholesterol Absorption [PE],Dietary Cholesterol Absorption Inhibitor [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-10-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20170126",
"EndMarketingDatePackage": "20190930",
"SamplePackage": "N"
}
}