{
"NDC": {
"NDCCode": "55700-710-30",
"PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (55700-710-30) ",
"NDC11Code": "55700-0710-30",
"ProductNDC": "55700-710",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Imipramine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Imipramine Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20181214",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA040903",
"LabelerName": "Quality Care Products, LLC",
"SubstanceName": "IMIPRAMINE HYDROCHLORIDE",
"StrengthNumber": "25",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Tricyclic Antidepressant [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-07-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20181214",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}