{
"NDC": {
"NDCCode": "55253-601-30",
"PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (55253-601-30)",
"NDC11Code": "55253-0601-30",
"ProductNDC": "55253-601",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Tiagabine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Tiagabine Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20121221",
"EndMarketingDate": "20170831",
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA020646",
"LabelerName": "CIMA LABS INC.",
"SubstanceName": "TIAGABINE HYDROCHLORIDE",
"StrengthNumber": "4",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Anti-epileptic Agent [EPC],Decreased Central Nervous System Disorganized Electrical Activity [PE]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-09-01",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}