{
"NDC": {
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"PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-796-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-796-01) ",
"NDC11Code": "51079-0796-20",
"ProductNDC": "51079-796",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Hydroxyzine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Hydroxyzine Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20100813",
"EndMarketingDate": "20190731",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA091176",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "HYDROXYZINE HYDROCHLORIDE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antihistamine [EPC],Histamine Receptor Antagonists [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-08-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20100813",
"EndMarketingDatePackage": "20190731",
"SamplePackage": "N"
}
}