{
"NDC": {
"NDCCode": "59762-0152-1",
"PackageDescription": "100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (59762-0152-1)",
"NDC11Code": "59762-0152-01",
"ProductNDC": "59762-0152",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Trandolapril And Verapamil Hydrochloride",
"ProprietaryNameSuffix": "Er",
"NonProprietaryName": "Trandolapril And Verapamil Hydrochloride",
"DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20150225",
"EndMarketingDate": "20180228",
"MarketingCategoryName": "NDA",
"ApplicationNumber": "NDA020591",
"LabelerName": "Greenstone LLC",
"SubstanceName": "TRANDOLAPRIL; VERAPAMIL HYDROCHLORIDE",
"StrengthNumber": "1; 240",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 3A Inhibitors [MoA],P-Glycoprotein Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-03-01",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}