{
"NDC": {
"NDCCode": "42291-805-30",
"PackageDescription": "30 TABLET in 1 BOTTLE (42291-805-30) ",
"NDC11Code": "42291-0805-30",
"ProductNDC": "42291-805",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Terbinafine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Terbinafine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20111020",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077919",
"LabelerName": "AvKARE, Inc.",
"SubstanceName": "TERBINAFINE HYDROCHLORIDE",
"StrengthNumber": "250",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-04-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20111020",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}