{
"NDC": {
"NDCCode": "42292-011-06",
"PackageDescription": "50 BLISTER PACK in 1 CARTON (42292-011-06) > 1 TABLET, FILM COATED in 1 BLISTER PACK (42292-011-01) ",
"NDC11Code": "42292-0011-06",
"ProductNDC": "42292-011",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Hydroxychloroquine Sulfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Hydroxychloroquine Sulfate",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ENTERAL",
"StartMarketingDate": "20160328",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040274",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "HYDROXYCHLOROQUINE SULFATE",
"StrengthNumber": "200",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antirheumatic Agent [EPC],Antimalarial [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-12-30",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20211231",
"StartMarketingDatePackage": "20160328",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}