{
"NDC": {
"NDCCode": "42291-552-60",
"PackageDescription": "60 TABLET, FILM COATED in 1 BOTTLE (42291-552-60) ",
"NDC11Code": "42291-0552-60",
"ProductNDC": "42291-552",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Memantine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Memantine",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20160111",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA090041",
"LabelerName": "AvKARE, Inc.",
"SubstanceName": "MEMANTINE HYDROCHLORIDE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "NMDA Receptor Antagonists [MoA],N-methyl-D-aspartate Receptor Antagonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-07-25",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20160111",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}