{
"NDC": {
"NDCCode": "35356-243-30",
"PackageDescription": "30 TABLET in 1 BOTTLE, PLASTIC (35356-243-30)",
"NDC11Code": "35356-0243-30",
"ProductNDC": "35356-243",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Terbinafine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Terbinafine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20100916",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA077919",
"LabelerName": "Lake Erie Medical DBA Quality Care Products LLC",
"SubstanceName": "TERBINAFINE HYDROCHLORIDE",
"StrengthNumber": "250",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Allylamine [Chemical/Ingredient],Allylamine Antifungal [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2016-12-22",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}