{
"NDC": {
"NDCCode": "72162-1475-0",
"PackageDescription": "1000 TABLET in 1 BOTTLE (72162-1475-0) ",
"NDC11Code": "72162-1475-00",
"ProductNDC": "72162-1475",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Imipramine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Imipramine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "19831021",
"EndMarketingDate": "20240831",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA088262",
"LabelerName": "Bryant Ranch Prepack",
"SubstanceName": "IMIPRAMINE HYDROCHLORIDE",
"StrengthNumber": "25",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Tricyclic Antidepressant [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-09-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20240206",
"EndMarketingDatePackage": "20240831",
"SamplePackage": "N"
}
}