{
"NDC": {
"NDCCode": "60687-184-57",
"PackageDescription": "60 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-184-57) / 1 TABLET in 1 BLISTER PACK (60687-184-11) ",
"NDC11Code": "60687-0184-57",
"ProductNDC": "60687-184",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Memantine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Memantine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20150909",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA090048",
"LabelerName": "American Health Packaging",
"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": "2025-04-24",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20150909",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}