{
"NDC": {
"NDCCode": "53746-925-60",
"PackageDescription": "60 TABLET in 1 BOTTLE (53746-925-60) ",
"NDC11Code": "53746-0925-60",
"ProductNDC": "53746-925",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Lacosamide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Lacosamide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20230517",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA204857",
"LabelerName": "Amneal Pharmaceuticals of New York LLC",
"SubstanceName": "LACOSAMIDE",
"StrengthNumber": "150",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Decreased Central Nervous System Disorganized Electrical Activity [PE]",
"DEASchedule": "CV",
"Status": "Active",
"LastUpdate": "2024-06-12",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20230517",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}