{
"NDC": {
"NDCCode": "16714-501-03",
"PackageDescription": "500 TABLET in 1 BOTTLE, PLASTIC (16714-501-03)",
"NDC11Code": "16714-0501-03",
"ProductNDC": "16714-501",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Terbinafine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Terbinafine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20090915",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078163",
"LabelerName": "Northstar Rx LLC",
"SubstanceName": "TERBINAFINE HYDROCHLORIDE",
"StrengthNumber": "250",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2016-12-02",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}