{
"NDC": {
"NDCCode": "71610-011-18",
"PackageDescription": "3000 TABLET in 1 BOTTLE (71610-011-18) ",
"NDC11Code": "71610-0011-18",
"ProductNDC": "71610-011",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Memantine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Memantine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20150401",
"EndMarketingDate": null,
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA021487",
"LabelerName": "Aphena Pharma Solutions - Tennessee, LLC",
"SubstanceName": "MEMANTINE HYDROCHLORIDE",
"StrengthNumber": "10",
"StrengthUnit": "mg/1",
"Pharm_Classes": "N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2017-12-07",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20171115",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}