{
"NDC": {
"NDCCode": "55154-5481-0",
"PackageDescription": "10 BLISTER PACK in 1 BAG (55154-5481-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK",
"NDC11Code": "55154-5481-00",
"ProductNDC": "55154-5481",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Diltiazem Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Diltiazem Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "19921105",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA072837",
"LabelerName": "Cardinal Health",
"SubstanceName": "DILTIAZEM HYDROCHLORIDE",
"StrengthNumber": "90",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Calcium Channel Antagonists [MoA],Calcium Channel Blocker [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-05-15",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}