{
"NDC": {
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"PackageDescription": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-265-32) / 1 CAPSULE in 1 BLISTER PACK (60687-265-33) ",
"NDC11Code": "60687-0265-32",
"ProductNDC": "60687-265",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Nortriptyline Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Nortriptyline Hydrochloride",
"DosageFormName": "CAPSULE",
"RouteName": "ORAL",
"StartMarketingDate": "20170124",
"EndMarketingDate": "20231031",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075520",
"LabelerName": "American Health Packaging",
"SubstanceName": "NORTRIPTYLINE HYDROCHLORIDE",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Tricyclic Antidepressant [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-11-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20170124",
"EndMarketingDatePackage": "20231031",
"SamplePackage": "N"
}
}