{
"NDC": {
"NDCCode": "60687-144-25",
"PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-144-25) > 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-144-95)",
"NDC11Code": "60687-0144-25",
"ProductNDC": "60687-144",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Amitriptyline Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Amitriptyline Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20150331",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040218",
"LabelerName": "American Health Packaging",
"SubstanceName": "AMITRIPTYLINE HYDROCHLORIDE",
"StrengthNumber": "100",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Tricyclic Antidepressant [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2017-02-13",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": null,
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}