{
"NDC": {
"NDCCode": "55154-5523-0",
"PackageDescription": "10 BLISTER PACK in 1 BAG (55154-5523-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK",
"NDC11Code": "55154-5523-00",
"ProductNDC": "55154-5523",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Diltiazem Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Diltiazem Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "19921105",
"EndMarketingDate": "20210131",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA073186",
"LabelerName": "Cardinal Health",
"SubstanceName": "DILTIAZEM HYDROCHLORIDE",
"StrengthNumber": "60",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-02-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "19921105",
"EndMarketingDatePackage": "20210131",
"SamplePackage": "N"
}
}