{
"NDC": {
"NDCCode": "68180-120-01",
"PackageDescription": "100 TABLET, FILM COATED in 1 BOTTLE (68180-120-01) ",
"NDC11Code": "68180-0120-01",
"ProductNDC": "68180-120",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Hydroxychloroquinesulfate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Hydroxychloroquinesulfate",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20180706",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA210543",
"LabelerName": "Lupin Pharmaceuticals, Inc.",
"SubstanceName": "HYDROXYCHLOROQUINE SULFATE",
"StrengthNumber": "200",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Antirheumatic Agent [EPC],Antimalarial [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-12-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20180706",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}