{
"NDC": {
"NDCCode": "51079-133-20",
"PackageDescription": "100 BLISTER PACK in 1 CARTON (51079-133-20) > 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-133-01) ",
"NDC11Code": "51079-0133-20",
"ProductNDC": "51079-133",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Amitriptyline Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Amitriptyline Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "19941026",
"EndMarketingDate": "20210131",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA086009",
"LabelerName": "Mylan Institutional Inc.",
"SubstanceName": "AMITRIPTYLINE HYDROCHLORIDE",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Tricyclic Antidepressant [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-02-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "19941026",
"EndMarketingDatePackage": "20210131",
"SamplePackage": "N"
}
}