{
"NDC": {
"NDCCode": "42292-008-03",
"PackageDescription": "30 BLISTER PACK in 1 CARTON (42292-008-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK (42292-008-01) ",
"NDC11Code": "42292-0008-03",
"ProductNDC": "42292-008",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Linezolid",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Linezolid",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20151216",
"EndMarketingDate": "20190531",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078845",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "LINEZOLID",
"StrengthNumber": "600",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Oxazolidinone Antibacterial [EPC],Oxazolidinones [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-06-04",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20151216",
"EndMarketingDatePackage": "20190531",
"SamplePackage": "N"
}
}